Item | Value |
---|---|
geneid | 23353 |
ensemblid | ENSG00000164828.18 |
hgncid | 18587 |
symbol | SUN1 |
name | Sad1 and UNC84 domain containing 1 |
refseq_nuc | NM_001130965.3 |
refseq_prot | NP_001124437.1 |
ensembl_nuc | ENST00000401592.6 |
ensembl_prot | ENSP00000384015.1 |
mane_status | MANE Select |
chr | chr7 |
start | 832476 |
end | 874934 |
strand | + |
ver | v1.2 |
region | chr7:832476-874934 |
region5000 | chr7:827476-879934 |
regionname0 | SUN1_chr7_832476_874934 |
regionname5000 | SUN1_chr7_827476_879934 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 785 | 191 | 48 | 34 | 85 | 5 | 19 | 67 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0002 | 1/1 | 785 | 123 | 25 | 24 | 50 | 6 | 16 | 36 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0003 | 0/0 | 785 | 64 | 8 | 15 | 27 | 3 | 11 | 21 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0004 | 0/0 | 785 | 10 | 0 | 0 | 10 | 0 | 0 | 5 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0005 | 0/0 | 785 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0006 | 0/0 | 785 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0007 | 0/0 | 785 | 3 | 1 | 0 | 2 | 0 | 0 | 2 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0008 | 0/0 | 785 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0009 | 0/0 | 785 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0010 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0011 | 0/0 | 785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0012 | 0/0 | 785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0013 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0014 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0015 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0016 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0017 | 0/0 | 785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0018 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0019 | 0/0 | 296 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(291): Show |
chr7 | 827476 | 879934 |
a0020 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
a0021 | 0/0 | 785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | MDFSR others(780): Show |
chr7 | 827476 | 879934 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2355 | 141 | 34 | 32 | 53 | 5 | 17 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0001c0004 | 0/0 | 2355 | 33 | 0 | 0 | 32 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0001c0006 | 0/0 | 2355 | 13 | 12 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0001c0022 | 0/0 | 2355 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0001c0023 | 0/0 | 2355 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0001c0024 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0001c0025 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0002c0002 | 0/1 | 2355 | 94 | 22 | 17 | 48 | 2 | 4 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0002c0005 | 1/0 | 2355 | 29 | 3 | 7 | 2 | 4 | 12 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0003c0003 | 0/0 | 2355 | 61 | 7 | 13 | 27 | 3 | 11 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0003c0012 | 0/0 | 2355 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0003c0021 | 0/0 | 2355 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0004c0007 | 0/0 | 2355 | 10 | 0 | 0 | 10 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0005c0008 | 0/0 | 2355 | 6 | 5 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0006c0009 | 0/0 | 2355 | 5 | 5 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0007c0010 | 0/0 | 2355 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0007c0031 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0008c0011 | 0/0 | 2355 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0009c0013 | 0/0 | 2355 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0010c0026 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0011c0019 | 0/0 | 2355 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0012c0030 | 0/0 | 2355 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0013c0020 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0014c0016 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0015c0028 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0016c0018 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0017c0027 | 0/0 | 2355 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0018c0017 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0019c0015 | 0/0 | 2336 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2331): Show |
chr7 | 827476 | 879934 | ||
a0020c0014 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 | ||
a0021c0029 | 0/0 | 2355 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ATGGA others(2350): Show |
chr7 | 827476 | 879934 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4010 | 131 | 31 | 27 | 52 | 4 | 17 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0011 | 0/0 | 4010 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0013 | 0/0 | 4010 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0015 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0016 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0017 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0019 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0021 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0001t0024 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0004t0002 | 0/0 | 4010 | 30 | 0 | 0 | 29 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0004t0008 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0004t0022 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0004t0023 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0006t0001 | 0/0 | 4010 | 10 | 10 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0006t0012 | 0/0 | 4010 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0006t0018 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0022t0001 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0023t0001 | 0/0 | 4010 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0024t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0001c0025t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0002c0002t0001 | 0/1 | 4010 | 82 | 20 | 17 | 38 | 2 | 4 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0002c0002t0003 | 0/0 | 4010 | 10 | 0 | 0 | 10 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0002c0002t0009 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0002c0005t0001 | 1/0 | 4010 | 29 | 3 | 7 | 2 | 4 | 12 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0003c0003t0001 | 0/0 | 4010 | 54 | 2 | 12 | 27 | 2 | 11 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0003c0003t0005 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0003c0003t0007 | 0/0 | 4010 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0003c0003t0010 | 0/0 | 4010 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0003c0012t0005 | 0/0 | 4010 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0003c0021t0020 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0004c0007t0001 | 0/0 | 4010 | 4 | 0 | 0 | 4 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0004c0007t0004 | 0/0 | 4010 | 6 | 0 | 0 | 6 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0005c0008t0001 | 0/0 | 4010 | 6 | 5 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0006c0009t0001 | 0/0 | 4010 | 5 | 5 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0007c0010t0001 | 0/0 | 4010 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0007c0031t0014 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0008c0011t0006 | 0/0 | 4010 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0009c0013t0001 | 0/0 | 4010 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0010c0026t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0011c0019t0001 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0012c0030t0001 | 0/0 | 4010 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0013c0020t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0014c0016t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0015c0028t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0016c0018t0006 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0017c0027t0001 | 0/0 | 4010 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0018c0017t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0019c0015t0008 | 0/0 | 3991 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(3986): Show |
chr7 | 827476 | 879934 |
a0020c0014t0002 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
a0021c0029t0001 | 0/0 | 4010 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | ACTCT others(4005): Show |
chr7 | 827476 | 879934 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 2 | 0 | 5 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0005 | 0/0 | 7 | 0 | 3 | 1 | 2 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0007 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0030 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0031 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0011g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0011g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0013g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0013g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0016g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0017g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0019g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0021g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0001t0024g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0008g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0022g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0004t0023g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0012g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0012g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0006t0018g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0022t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0023t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0024t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0001c0025t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0001 | 0/0 | 9 | 0 | 8 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0258 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0006 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0009g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0002t0009g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0004 | 0/0 | 6 | 1 | 1 | 0 | 3 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0023 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0042 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0002c0005t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0017 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0321 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0323 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0005g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0005g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0007g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0007g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0007g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0010g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0003t0010g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0012t0005g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0012t0005g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0003c0021t0020g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0004c0007t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0016 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0005c0008t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0006c0009t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0007c0010t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0007c0010t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0007c0031t0014g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0008c0011t0006g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0008c0011t0006g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0009c0013t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0009c0013t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0010c0026t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0011c0019t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0012c0030t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0013c0020t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0014c0016t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0015c0028t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0016c0018t0006g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0017c0027t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0018c0017t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0019c0015t0008g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0020c0014t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
a0021c0029t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00099 | hp2 | a0002 | c0005 | t0001 | g0004 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00140 | hp1 | a0002 | c0002 | t0001 | g0253 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00140 | hp2 | a0002 | c0005 | t0001 | g0052 | EUR | GBR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00323 | hp1 | a0001 | c0001 | t0011 | g0335 | EUR | FIN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00323 | hp2 | a0003 | c0003 | t0010 | g0326 | EUR | FIN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00408 | hp2 | a0010 | c0026 | t0001 | g0197 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00423 | hp2 | a0004 | c0007 | t0004 | g0187 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00438 | hp1 | a0004 | c0007 | t0004 | g0012 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00438 | hp2 | a0004 | c0007 | t0001 | g0029 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00544 | hp2 | a0001 | c0004 | t0002 | g0014 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00558 | hp2 | a0003 | c0003 | t0001 | g0328 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00621 | hp1 | a0001 | c0004 | t0002 | g0228 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00639 | hp2 | a0003 | c0003 | t0001 | g0327 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00642 | hp1 | a0001 | c0001 | t0011 | g0167 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00642 | hp2 | a0003 | c0003 | t0010 | g0325 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00673 | hp2 | a0004 | c0007 | t0001 | g0145 | EAS | CHS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00735 | hp1 | a0001 | c0001 | t0019 | g0026 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00735 | hp2 | a0003 | c0003 | t0001 | g0017 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00738 | hp1 | a0002 | c0005 | t0001 | g0023 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01069 | hp1 | a0003 | c0003 | t0001 | g0316 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01074 | hp1 | a0003 | c0003 | t0001 | g0277 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01074 | hp2 | a0011 | c0019 | t0001 | g0004 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0267 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0255 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01099 | hp2 | a0002 | c0005 | t0001 | g0095 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01106 | hp1 | a0003 | c0012 | t0005 | g0275 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01109 | hp1 | a0002 | c0002 | t0001 | g0254 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01109 | hp2 | a0001 | c0022 | t0001 | g0156 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01167 | hp1 | a0002 | c0005 | t0001 | g0094 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01168 | hp2 | a0001 | c0001 | t0013 | g0003 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01169 | hp1 | a0001 | c0001 | t0013 | g0170 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01169 | hp2 | a0002 | c0005 | t0001 | g0004 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01175 | hp2 | a0001 | c0001 | t0017 | g0162 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01243 | hp1 | a0005 | c0008 | t0001 | g0016 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01243 | hp2 | a0001 | c0006 | t0012 | g0044 | AMR | PUR | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01255 | hp2 | a0002 | c0005 | t0001 | g0009 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01256 | hp1 | a0002 | c0005 | t0001 | g0009 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01258 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0257 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01346 | hp2 | a0002 | c0005 | t0001 | g0009 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01358 | hp1 | a0003 | c0021 | t0020 | g0300 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01361 | hp1 | a0003 | c0003 | t0001 | g0285 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01433 | hp2 | a0003 | c0003 | t0001 | g0314 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01496 | hp2 | a0012 | c0030 | t0001 | g0051 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01515 | hp1 | a0003 | c0003 | t0001 | g0324 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01515 | hp2 | a0002 | c0005 | t0001 | g0004 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01517 | hp1 | a0003 | c0003 | t0001 | g0323 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01884 | hp1 | a0002 | c0005 | t0001 | g0023 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01884 | hp2 | a0005 | c0008 | t0001 | g0036 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01891 | hp1 | a0013 | c0020 | t0001 | g0252 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01928 | hp1 | a0003 | c0003 | t0001 | g0017 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01943 | hp2 | a0003 | c0003 | t0001 | g0315 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0251 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0296 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01993 | hp2 | a0002 | c0002 | t0001 | g0256 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02015 | hp1 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02040 | hp2 | a0003 | c0003 | t0001 | g0291 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02055 | hp2 | a0005 | c0008 | t0001 | g0266 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02056 | hp1 | a0001 | c0004 | t0002 | g0216 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02056 | hp2 | a0003 | c0003 | t0001 | g0280 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02071 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02071 | hp2 | a0002 | c0005 | t0001 | g0027 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02074 | hp2 | a0003 | c0003 | t0001 | g0282 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02080 | hp1 | a0014 | c0016 | t0001 | g0334 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02083 | hp1 | a0004 | c0007 | t0001 | g0029 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02083 | hp2 | a0003 | c0003 | t0001 | g0297 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02129 | hp1 | a0002 | c0005 | t0001 | g0027 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02132 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02132 | hp2 | a0001 | c0004 | t0002 | g0219 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02135 | hp1 | a0003 | c0003 | t0001 | g0287 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02145 | hp2 | a0001 | c0024 | t0001 | g0154 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02148 | hp1 | a0003 | c0003 | t0001 | g0310 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0001 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CDX | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02257 | hp1 | a0001 | c0025 | t0001 | g0200 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02257 | hp2 | a0001 | c0006 | t0001 | g0058 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02258 | hp1 | a0003 | c0003 | t0001 | g0281 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02258 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02273 | hp2 | a0003 | c0003 | t0001 | g0017 | AMR | PEL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02523 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | KHV | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02572 | hp1 | a0006 | c0009 | t0001 | g0099 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02572 | hp2 | a0001 | c0001 | t0024 | g0212 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02602 | hp1 | a0002 | c0005 | t0001 | g0089 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02602 | hp2 | a0003 | c0003 | t0001 | g0318 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02615 | hp1 | a0003 | c0012 | t0005 | g0274 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02615 | hp2 | a0001 | c0006 | t0018 | g0260 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02622 | hp2 | a0006 | c0009 | t0001 | g0101 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0248 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02630 | hp2 | a0006 | c0009 | t0001 | g0100 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02698 | hp2 | a0002 | c0005 | t0001 | g0090 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02717 | hp1 | a0001 | c0006 | t0012 | g0043 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0245 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02723 | hp2 | a0008 | c0011 | t0006 | g0269 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02735 | hp1 | a0003 | c0003 | t0001 | g0320 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02735 | hp2 | a0002 | c0005 | t0001 | g0004 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02738 | hp2 | a0003 | c0003 | t0001 | g0319 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0250 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02809 | hp2 | a0005 | c0008 | t0001 | g0016 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0249 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02818 | hp2 | a0002 | c0002 | t0001 | g0015 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0268 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02895 | hp2 | a0003 | c0003 | t0005 | g0273 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02896 | hp1 | a0003 | c0003 | t0007 | g0311 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02896 | hp2 | a0002 | c0002 | t0001 | g0259 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02897 | hp2 | a0003 | c0003 | t0007 | g0313 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02922 | hp1 | a0006 | c0009 | t0001 | g0018 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02965 | hp2 | a0001 | c0006 | t0001 | g0019 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02970 | hp1 | a0005 | c0008 | t0001 | g0016 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0055 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03017 | hp2 | a0003 | c0003 | t0001 | g0293 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0056 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03041 | hp2 | a0001 | c0001 | t0021 | g0121 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03098 | hp1 | a0016 | c0018 | t0006 | g0270 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03130 | hp1 | a0008 | c0011 | t0006 | g0271 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0246 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03195 | hp1 | a0001 | c0006 | t0001 | g0057 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03209 | hp2 | a0002 | c0002 | t0001 | g0061 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03225 | hp1 | a0002 | c0002 | t0001 | g0062 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03225 | hp2 | a0001 | c0006 | t0001 | g0054 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0035 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03239 | hp2 | a0001 | c0023 | t0001 | g0008 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03453 | hp2 | a0007 | c0031 | t0014 | g0262 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03486 | hp1 | a0001 | c0006 | t0001 | g0102 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03490 | hp1 | a0002 | c0005 | t0001 | g0087 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03491 | hp1 | a0002 | c0002 | t0001 | g0077 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03491 | hp2 | a0003 | c0003 | t0001 | g0332 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03492 | hp1 | a0002 | c0005 | t0001 | g0086 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03492 | hp2 | a0003 | c0003 | t0001 | g0331 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03516 | hp1 | a0017 | c0027 | t0001 | g0059 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03516 | hp2 | a0006 | c0009 | t0001 | g0018 | AFR | ESN | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03540 | hp2 | a0002 | c0002 | t0001 | g0247 | AFR | GWD | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03579 | hp1 | a0002 | c0002 | t0001 | g0015 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03579 | hp2 | a0003 | c0003 | t0007 | g0312 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03669 | hp1 | a0002 | c0005 | t0001 | g0093 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03669 | hp2 | a0003 | c0003 | t0001 | g0298 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03688 | hp2 | a0002 | c0005 | t0001 | g0092 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03704 | hp1 | a0003 | c0003 | t0001 | g0299 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0071 | SAS | PJL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0001 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03927 | hp1 | a0001 | c0004 | t0002 | g0227 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04115 | hp1 | a0002 | c0005 | t0001 | g0098 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04115 | hp2 | a0003 | c0003 | t0001 | g0321 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04184 | hp1 | a0003 | c0003 | t0001 | g0302 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04199 | hp2 | a0002 | c0005 | t0001 | g0097 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04204 | hp1 | a0002 | c0005 | t0001 | g0091 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04204 | hp2 | a0002 | c0005 | t0001 | g0088 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04228 | hp1 | a0002 | c0005 | t0001 | g0096 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0164 | SAS | STU | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18522 | hp1 | a0003 | c0003 | t0001 | g0330 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18522 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18612 | hp1 | a0001 | c0004 | t0002 | g0233 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18747 | hp1 | a0018 | c0017 | t0001 | g0309 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18906 | hp1 | a0005 | c0008 | t0001 | g0036 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18939 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18940 | hp2 | a0004 | c0007 | t0004 | g0012 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18941 | hp2 | a0001 | c0004 | t0002 | g0229 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18943 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18944 | hp1 | a0001 | c0001 | t0015 | g0115 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18944 | hp2 | a0002 | c0002 | t0003 | g0085 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18945 | hp2 | a0001 | c0004 | t0002 | g0225 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18946 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18946 | hp2 | a0003 | c0003 | t0001 | g0301 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18947 | hp1 | a0001 | c0004 | t0002 | g0232 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18950 | hp1 | a0001 | c0004 | t0002 | g0240 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18950 | hp2 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18951 | hp2 | a0009 | c0013 | t0001 | g0163 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18952 | hp2 | a0004 | c0007 | t0004 | g0120 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18954 | hp1 | a0003 | c0003 | t0001 | g0317 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18957 | hp2 | a0001 | c0004 | t0002 | g0218 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18959 | hp1 | a0003 | c0003 | t0001 | g0329 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18960 | hp1 | a0001 | c0004 | t0002 | g0237 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18961 | hp1 | a0002 | c0002 | t0003 | g0205 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18962 | hp1 | a0001 | c0004 | t0002 | g0217 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18963 | hp1 | a0004 | c0007 | t0004 | g0012 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18963 | hp2 | a0007 | c0010 | t0001 | g0132 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0067 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18965 | hp1 | a0003 | c0003 | t0001 | g0304 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18967 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18967 | hp2 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0308 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18970 | hp2 | a0002 | c0002 | t0001 | g0010 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18972 | hp1 | a0001 | c0004 | t0002 | g0242 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18972 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18973 | hp1 | a0003 | c0003 | t0001 | g0278 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18973 | hp2 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18977 | hp2 | a0007 | c0010 | t0001 | g0201 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18978 | hp1 | a0003 | c0003 | t0001 | g0290 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18978 | hp2 | a0001 | c0004 | t0023 | g0241 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18979 | hp1 | a0001 | c0004 | t0008 | g0244 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18979 | hp2 | a0003 | c0003 | t0001 | g0292 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18980 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18982 | hp2 | a0001 | c0004 | t0002 | g0238 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18983 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18984 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18988 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18990 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18993 | hp1 | a0003 | c0003 | t0001 | g0037 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18999 | hp1 | a0001 | c0004 | t0002 | g0231 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0048 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19000 | hp1 | a0004 | c0007 | t0004 | g0146 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19002 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19002 | hp2 | a0003 | c0003 | t0001 | g0286 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19005 | hp1 | a0001 | c0004 | t0002 | g0014 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19006 | hp2 | a0001 | c0004 | t0022 | g0221 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19007 | hp1 | a0001 | c0004 | t0002 | g0014 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19009 | hp1 | a0003 | c0003 | t0001 | g0283 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0305 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19012 | hp1 | a0001 | c0004 | t0002 | g0013 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19012 | hp2 | a0002 | c0002 | t0003 | g0073 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19030 | hp2 | a0002 | c0002 | t0009 | g0040 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19043 | hp1 | a0001 | c0001 | t0016 | g0264 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19043 | hp2 | a0001 | c0006 | t0001 | g0046 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19055 | hp1 | a0003 | c0003 | t0001 | g0295 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19055 | hp2 | a0019 | c0015 | t0008 | g0235 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19056 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19056 | hp2 | a0020 | c0014 | t0002 | g0239 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19057 | hp1 | a0003 | c0003 | t0001 | g0289 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19057 | hp2 | a0009 | c0013 | t0001 | g0124 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19058 | hp2 | a0003 | c0003 | t0001 | g0303 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19062 | hp1 | a0001 | c0004 | t0002 | g0224 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19064 | hp1 | a0001 | c0004 | t0002 | g0236 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19068 | hp1 | a0002 | c0002 | t0003 | g0022 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19068 | hp2 | a0001 | c0004 | t0002 | g0230 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19070 | hp1 | a0003 | c0003 | t0001 | g0288 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19074 | hp1 | a0003 | c0003 | t0001 | g0307 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19077 | hp1 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19077 | hp2 | a0021 | c0029 | t0001 | g0141 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19079 | hp1 | a0001 | c0004 | t0002 | g0223 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19079 | hp2 | a0003 | c0003 | t0001 | g0276 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19080 | hp1 | a0004 | c0007 | t0001 | g0178 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19080 | hp2 | a0001 | c0004 | t0002 | g0243 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19081 | hp1 | a0001 | c0004 | t0002 | g0222 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0294 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19085 | hp1 | a0002 | c0002 | t0003 | g0006 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19086 | hp2 | a0001 | c0004 | t0002 | g0234 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0066 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19088 | hp1 | a0001 | c0004 | t0002 | g0220 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19088 | hp2 | a0003 | c0003 | t0001 | g0306 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19091 | hp2 | a0002 | c0002 | t0001 | g0081 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19240 | hp1 | a0002 | c0002 | t0009 | g0039 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | YRI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20129 | hp1 | a0001 | c0006 | t0001 | g0045 | AFR | ASW | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ASW | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20752 | hp2 | a0002 | c0002 | t0001 | g0065 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20805 | hp1 | a0002 | c0005 | t0001 | g0004 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0126 | SAS | GIH | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20905 | hp2 | a0003 | c0003 | t0001 | g0322 | SAS | GIH | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG01123 | hp2 | a0003 | c0003 | t0001 | g0284 | AMR | CLM | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02486 | hp1 | a0002 | c0005 | t0001 | g0053 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02559 | hp1 | a0015 | c0028 | t0001 | g0060 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03471 | hp1 | a0001 | c0006 | t0001 | g0019 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | MSL | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0038 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18955 | hp1 | a0001 | c0004 | t0002 | g0226 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20300 | hp1 | a0002 | c0005 | t0001 | g0004 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | USA | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA21309 | hp1 | a0003 | c0003 | t0005 | g0272 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | LWK | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
homoSapiens | chm13v2 | a0002 | c0002 | t0001 | g0258 | REF | REF | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
homoSapiens | grch38p0 | a0002 | c0005 | t0001 | g0042 | REF | REF | SUN1_chr7_827476_879934 | SUN1 | chr7 | 827476 | 879934 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:838923 | G | A | 1 | a0020 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.203G>A | p.Gly68Asp | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 252/4010 | 203/2358 | 68/785 | chr7 | 838923 | |||
chr7:838946 | G | T | 1 | a0007 | 1 | HG03453.hp2 | missense_variant | MODERATE | c.226G>T | p.Gly76Cys | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 275/4010 | 226/2358 | 76/785 | chr7 | 838946 | |||
chr7:838947 | G | C | 1 | a0007 | 2 | NA18963.hp2 NA18977.hp2 |
missense_variant | MODERATE | c.227G>C | p.Gly76Ala | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 276/4010 | 227/2358 | 76/785 | chr7 | 838947 | |||
chr7:838977 | G | C | 1 | a0014 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.257G>C | p.Arg86Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 306/4010 | 257/2358 | 86/785 | chr7 | 838977 | |||
chr7:841957 | A | C | 1 | a0006 | 5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
missense_variant | MODERATE | c.278A>C | p.Gln93Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 327/4010 | 278/2358 | 93/785 | chr7 | 841957 | |||
chr7:841960 | G | A | 1 | a0018 | 1 | NA18747.hp1 | missense_variant | MODERATE | c.281G>A | p.Arg94His | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 330/4010 | 281/2358 | 94/785 | chr7 | 841960 | |||
chr7:842031 | C | T | 13 | a0001 a0004 a0005 others(10): Show |
220 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(217): Show |
missense_variant | MODERATE | c.352C>T | p.His118Tyr | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 401/4010 | 352/2358 | 118/785 | chr7 | 842031 | |||
chr7:843451 | G | A | 2 | a0008 a0016 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
missense_variant | MODERATE | c.589G>A | p.Val197Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/19 | 638/4010 | 589/2358 | 197/785 | chr7 | 843451 | |||
chr7:851470 | G | A | 1 | a0009 | 2 | NA18951.hp2 NA19057.hp2 |
missense_variant | MODERATE | c.745G>A | p.Val249Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/19 | 794/4010 | 745/2358 | 249/785 | chr7 | 851470 | |||
chr7:852644 | TCATCCCA others(12): Show |
T | 1 | a0019 | 1 | NA19055.hp2 | frameshift_variant | HIGH | c.889_907delATCCCACT others(11): Show |
p.Ile297fs | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/19 | 938/4010 | 889/2358 | 297/785 | INFO_REALIGN_3_PRIME | chr7 | 852644 | ||
chr7:853488 | A | G | 1 | a0012 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.1133A>G | p.His378Arg | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/19 | 1182/4010 | 1133/2358 | 378/785 | chr7 | 853488 | |||
chr7:856386 | A | T | 1 | a0021 | 1 | NA19077.hp2 | missense_variant | MODERATE | c.1379A>T | p.Lys460Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/19 | 1428/4010 | 1379/2358 | 460/785 | chr7 | 856386 | |||
chr7:857859 | G | A | 3 | a0003 a0010 a0018 |
66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
missense_variant | MODERATE | c.1426G>A | p.Glu476Lys | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/19 | 1475/4010 | 1426/2358 | 476/785 | chr7 | 857859 | |||
chr7:860183 | G | T | 2 | a0004 a0021 |
11 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(8): Show |
missense_variant | MODERATE | c.1580G>T | p.Gly527Val | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1629/4010 | 1580/2358 | 527/785 | chr7 | 860183 | |||
chr7:860249 | C | T | 1 | a0005 | 6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
missense_variant | MODERATE | c.1646C>T | p.Thr549Met | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1695/4010 | 1646/2358 | 549/785 | chr7 | 860249 | |||
chr7:860279 | T | C | 1 | a0013 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1676T>C | p.Leu559Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1725/4010 | 1676/2358 | 559/785 | chr7 | 860279 | |||
chr7:860363 | C | T | 1 | a0015 | 1 | HG02559.hp1 | missense_variant | MODERATE | c.1760C>T | p.Ala587Val | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/19 | 1809/4010 | 1760/2358 | 587/785 | chr7 | 860363 | |||
chr7:861461 | G | A | 1 | a0016 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.1861G>A | p.Gly621Ser | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/19 | 1910/4010 | 1861/2358 | 621/785 | chr7 | 861461 | |||
chr7:869482 | A | G | 1 | a0017 | 1 | HG03516.hp1 | missense_variant | MODERATE | c.2114A>G | p.Asn705Ser | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/19 | 2163/4010 | 2114/2358 | 705/785 | chr7 | 869482 | |||
chr7:873317 | G | A | 1 | a0011 | 1 | HG01074.hp2 | missense_variant | MODERATE | c.2344G>A | p.Glu782Lys | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 2393/4010 | 2344/2358 | 782/785 | chr7 | 873317 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:838834 | G | A | 3 | a0001c0004 a0019c0015 a0020c0014 |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
synonymous_variant | LOW | c.114G>A | p.Thr38Thr | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/19 | 163/4010 | 114/2358 | 38/785 | chr7 | 838834 | |||
chr7:842045 | C | T | 1 | a0003c0021 | 1 | HG01358.hp1 | synonymous_variant | LOW | c.366C>T | p.Val122Val | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/19 | 415/4010 | 366/2358 | 122/785 | chr7 | 842045 | |||
chr7:843468 | C | T | 3 | a0003c0012 a0008c0011 a0016c0018 |
5 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(2): Show |
synonymous_variant | LOW | c.606C>T | p.Pro202Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/19 | 655/4010 | 606/2358 | 202/785 | chr7 | 843468 | |||
chr7:857831 | G | A | 1 | a0001c0022 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.1398G>A | p.Ala466Ala | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/19 | 1447/4010 | 1398/2358 | 466/785 | chr7 | 857831 | |||
chr7:857855 | A | G | 15 | a0001c0004 a0001c0006 a0002c0002 others(12): Show |
216 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(213): Show |
synonymous_variant | LOW | c.1422A>G | p.Thr474Thr | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/19 | 1471/4010 | 1422/2358 | 474/785 | chr7 | 857855 | |||
chr7:869411 | G | A | 3 | a0001c0004 a0019c0015 a0020c0014 |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
synonymous_variant | LOW | c.2043G>A | p.Arg681Arg | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/19 | 2092/4010 | 2043/2358 | 681/785 | chr7 | 869411 | |||
chr7:869435 | C | T | 1 | a0001c0025 | 1 | HG02257.hp1 | synonymous_variant | LOW | c.2067C>T | p.Ala689Ala | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/19 | 2116/4010 | 2067/2358 | 689/785 | chr7 | 869435 | |||
chr7:872560 | C | T | 1 | a0001c0024 | 1 | HG02145.hp2 | splice_region_variant&synonymous_variant | LOW | c.2239C>T | p.Leu747Leu | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/19 | 2288/4010 | 2239/2358 | 747/785 | chr7 | 872560 | |||
chr7:873223 | C | T | 1 | a0001c0023 | 1 | HG03239.hp2 | synonymous_variant | LOW | c.2250C>T | p.Pro750Pro | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 2299/4010 | 2250/2358 | 750/785 | chr7 | 873223 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:873355 | C | T | 1 | a0004c0007t0004 | 6 | HG00423.hp2 HG00438.hp1 NA18940.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*24C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 24 | chr7 | 873355 | ||||||
chr7:873419 | T | C | 2 | a0001c0004t0008 a0019c0015t0008 |
2 | NA18979.hp1 NA19055.hp2 |
3_prime_UTR_variant | MODIFIER | c.*88T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 88 | chr7 | 873419 | ||||||
chr7:873483 | C | T | 1 | a0003c0003t0007 | 3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*152C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 152 | chr7 | 873483 | ||||||
chr7:873495 | C | T | 1 | a0001c0001t0024 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*164C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 164 | chr7 | 873495 | ||||||
chr7:873554 | C | G | 1 | a0001c0001t0013 | 2 | HG01168.hp2 HG01169.hp1 |
3_prime_UTR_variant | MODIFIER | c.*223C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 223 | chr7 | 873554 | ||||||
chr7:873566 | G | A | 1 | a0007c0031t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*235G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 235 | chr7 | 873566 | ||||||
chr7:873580 | C | T | 1 | a0001c0004t0023 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*249C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 249 | chr7 | 873580 | ||||||
chr7:873592 | A | T | 1 | a0001c0004t0022 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*261A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 261 | chr7 | 873592 | ||||||
chr7:873594 | C | T | 1 | a0001c0006t0012 | 2 | HG01243.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*263C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 263 | chr7 | 873594 | ||||||
chr7:873595 | G | T | 4 | a0003c0003t0005 a0003c0012t0005 a0008c0011t0006 others(1): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*264G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 264 | chr7 | 873595 | ||||||
chr7:873815 | G | A | 6 | a0001c0004t0002 a0001c0004t0008 a0001c0004t0022 others(3): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*484G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 484 | chr7 | 873815 | ||||||
chr7:873844 | T | G | 1 | a0001c0006t0012 | 2 | HG01243.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*513T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 513 | chr7 | 873844 | ||||||
chr7:873874 | A | G | 1 | a0001c0001t0011 | 2 | HG00323.hp1 HG00642.hp1 |
3_prime_UTR_variant | MODIFIER | c.*543A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 543 | chr7 | 873874 | ||||||
chr7:873972 | T | G | 2 | a0003c0003t0005 a0003c0012t0005 |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*641T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 641 | chr7 | 873972 | ||||||
chr7:874100 | A | T | 1 | a0001c0001t0021 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*769A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 769 | chr7 | 874100 | ||||||
chr7:874111 | G | A | 1 | a0002c0002t0009 | 2 | NA19030.hp2 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*780G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 780 | chr7 | 874111 | ||||||
chr7:874124 | G | T | 1 | a0003c0021t0020 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*793G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 793 | chr7 | 874124 | ||||||
chr7:874161 | G | A | 1 | a0002c0002t0003 | 10 | NA18943.hp2 NA18944.hp2 NA18961.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*830G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 830 | chr7 | 874161 | ||||||
chr7:874215 | G | T | 1 | a0001c0001t0019 | 1 | HG00735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*884G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 884 | chr7 | 874215 | ||||||
chr7:874220 | C | T | 1 | a0001c0006t0018 | 1 | HG02615.hp2 | 3_prime_UTR_variant | MODIFIER | c.*889C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 889 | chr7 | 874220 | ||||||
chr7:874221 | G | A | 1 | a0003c0003t0010 | 2 | HG00323.hp2 HG00642.hp2 |
3_prime_UTR_variant | MODIFIER | c.*890G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 890 | chr7 | 874221 | ||||||
chr7:874370 | C | T | 1 | a0001c0001t0017 | 1 | HG01175.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1039C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1039 | chr7 | 874370 | ||||||
chr7:874849 | A | G | 1 | a0001c0001t0016 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1518A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1518 | chr7 | 874849 | ||||||
chr7:874899 | A | C | 1 | a0001c0001t0015 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1568A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1568 | chr7 | 874899 | ||||||
chr7:874916 | C | T | 1 | a0007c0031t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1585C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 19/19 | 1585 | chr7 | 874916 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:832618 | A | T | 1 | a0001c0001t0011g0335 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.77+17A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832618 | |||||||
chr7:832657 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.77+56G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832657 | |||||||
chr7:832661 | G | A | 1 | a0006c0009t0001g0018 | 2 | HG02922.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.77+60G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832661 | |||||||
chr7:832694 | C | T | 1 | a0014c0016t0001g0334 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77+93C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832694 | |||||||
chr7:832750 | T | G | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.77+149T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832750 | |||||||
chr7:832813 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.77+212G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832813 | |||||||
chr7:832875 | G | T | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.77+274G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832875 | |||||||
chr7:832993 | C | T | 1 | a0002c0002t0001g0333 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.77+392C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 832993 | |||||||
chr7:833021 | A | G | 66 | a0001c0001t0001g0279 a0003c0003t0001g0017 a0003c0003t0001g0037 others(63): Show |
69 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.77+420A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833021 | |||||||
chr7:833140 | A | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(259): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.77+539A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833140 | |||||||
chr7:833169 | A | G | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.77+568A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833169 | |||||||
chr7:833211 | G | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.77+610G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833211 | |||||||
chr7:833306 | C | CT | 136 | a0001c0001t0001g0279 a0001c0006t0001g0019 a0001c0006t0001g0045 others(133): Show |
166 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.77+719dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 833306 | ||||||
chr7:833306 | CT | C | 192 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(189): Show |
241 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.77+719delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 833306 | ||||||
chr7:833320 | T | C | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.77+719T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833320 | |||||||
chr7:833321 | C | G | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.77+720C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833321 | |||||||
chr7:833322 | G | T | 2 | a0001c0001t0001g0214 a0001c0001t0001g0215 |
2 | HG02155.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.77+721G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833322 | |||||||
chr7:833386 | C | A | 1 | a0001c0006t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.77+785C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833386 | |||||||
chr7:833467 | C | T | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(193): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.77+866C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833467 | |||||||
chr7:833477 | A | T | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.77+876A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833477 | |||||||
chr7:833483 | G | A | 1 | a0001c0006t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.77+882G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833483 | |||||||
chr7:833515 | G | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.77+914G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833515 | |||||||
chr7:833555 | C | T | 1 | a0001c0001t0001g0213 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.77+954C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833555 | |||||||
chr7:833758 | C | T | 166 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(163): Show |
211 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.77+1157C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833758 | |||||||
chr7:833776 | C | T | 1 | a0001c0001t0024g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.77+1175C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833776 | |||||||
chr7:833783 | C | T | 1 | a0002c0002t0001g0267 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.77+1182C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833783 | |||||||
chr7:833836 | TGCTGCTT others(6): Show |
T | 66 | a0001c0001t0001g0279 a0003c0003t0001g0017 a0003c0003t0001g0037 others(63): Show |
69 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.77+1237_77+1249del others(13): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 833836 | ||||||
chr7:833887 | T | C | 1 | a0002c0002t0001g0047 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.77+1286T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833887 | |||||||
chr7:833973 | A | G | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.77+1372A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 833973 | |||||||
chr7:834012 | C | G | 1 | a0001c0001t0001g0211 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.77+1411C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834012 | |||||||
chr7:834070 | T | TTGTAGGC others(46): Show |
128 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0008 others(125): Show |
152 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.77+1516_77+1568dup others(53): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834070 | ||||||
chr7:834070 | TTGTAGGC others(46): Show |
T | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.77+1516_77+1568del others(53): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834070 | ||||||
chr7:834117 | T | TGGATGGT others(46): Show |
11 | a0001c0001t0001g0005 a0001c0001t0001g0025 a0001c0001t0001g0026 others(8): Show |
18 | HG00099.hp1 HG00735.hp1 HG01070.hp2 others(15): Show |
intron_variant | MODIFIER | c.77+1597_77+1649dup others(53): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834117 | ||||||
chr7:834118 | G | A | 2 | a0002c0002t0001g0048 a0002c0002t0001g0049 |
2 | NA18984.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.77+1517G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834118 | |||||||
chr7:834150 | C | T | 4 | a0006c0009t0001g0018 a0006c0009t0001g0099 a0006c0009t0001g0100 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.77+1549C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834150 | |||||||
chr7:834224 | G | A | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+1623G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834224 | |||||||
chr7:834258 | C | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(262): Show |
317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.77+1657C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834258 | |||||||
chr7:834557 | A | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+1956A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834557 | |||||||
chr7:834607 | T | C | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.77+2006T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834607 | |||||||
chr7:834629 | G | C | 196 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(193): Show |
245 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.77+2028G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834629 | |||||||
chr7:834639 | C | T | 3 | a0001c0001t0001g0031 a0001c0001t0001g0209 a0001c0001t0001g0210 |
4 | HG01192.hp1 HG02055.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.77+2038C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834639 | |||||||
chr7:834661 | G | A | 4 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.77+2060G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834661 | |||||||
chr7:834736 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.77+2135G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834736 | |||||||
chr7:834775 | A | AT | 25 | a0001c0006t0001g0102 a0002c0002t0001g0001 a0002c0002t0001g0015 others(22): Show |
39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.77+2182dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 834775 | ||||||
chr7:834839 | G | C | 1 | a0002c0002t0009g0039 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.77+2238G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 834839 | |||||||
chr7:835002 | A | G | 100 | a0001c0001t0001g0279 a0001c0004t0002g0013 a0001c0004t0002g0014 others(97): Show |
107 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.77+2401A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835002 | |||||||
chr7:835095 | A | T | 66 | a0001c0001t0001g0279 a0003c0003t0001g0017 a0003c0003t0001g0037 others(63): Show |
69 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(66): Show |
intron_variant | MODIFIER | c.77+2494A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835095 | |||||||
chr7:835101 | T | G | 1 | a0002c0002t0001g0050 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.77+2500T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835101 | |||||||
chr7:835199 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.77+2598C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835199 | |||||||
chr7:835242 | CACGGGTT others(6): Show |
C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2642_77+2654del others(13): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835242 | |||||||
chr7:835256 | C | T | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2655C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835256 | |||||||
chr7:835257 | C | G | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2656C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835257 | |||||||
chr7:835259 | G | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.77+2658G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835259 | |||||||
chr7:835551 | T | C | 2 | a0001c0006t0018g0260 a0012c0030t0001g0051 |
2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.77+2950T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835551 | |||||||
chr7:835560 | A | T | 1 | a0014c0016t0001g0334 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.77+2959A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835560 | |||||||
chr7:835579 | C | G | 25 | a0001c0006t0001g0102 a0002c0002t0001g0001 a0002c0002t0001g0015 others(22): Show |
39 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(36): Show |
intron_variant | MODIFIER | c.77+2978C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835579 | |||||||
chr7:835748 | C | T | 2 | a0003c0003t0001g0331 a0003c0003t0001g0332 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.78-3050C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835748 | |||||||
chr7:835923 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.78-2875C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835923 | |||||||
chr7:835968 | G | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-2830G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 835968 | |||||||
chr7:836020 | G | A | 32 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(29): Show |
36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-2778G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836020 | |||||||
chr7:836026 | G | A | 3 | a0002c0005t0001g0009 a0002c0005t0001g0052 a0002c0005t0001g0053 |
5 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.78-2772G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836026 | |||||||
chr7:836034 | C | T | 1 | a0001c0004t0008g0244 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.78-2764C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836034 | |||||||
chr7:836147 | G | A | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(315): Show |
389 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(386): Show |
intron_variant | MODIFIER | c.78-2651G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836147 | |||||||
chr7:836240 | G | T | 1 | a0001c0001t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.78-2558G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836240 | |||||||
chr7:836305 | C | G | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-2493C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836305 | |||||||
chr7:836348 | C | T | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78-2450C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836348 | |||||||
chr7:836363 | A | G | 1 | a0001c0001t0001g0213 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.78-2435A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836363 | |||||||
chr7:836478 | A | C | 1 | a0001c0001t0001g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.78-2320A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836478 | |||||||
chr7:836590 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.78-2208C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836590 | |||||||
chr7:836888 | C | T | 63 | a0001c0001t0001g0279 a0003c0003t0001g0017 a0003c0003t0001g0037 others(60): Show |
66 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(63): Show |
intron_variant | MODIFIER | c.78-1910C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836888 | |||||||
chr7:836902 | C | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-1896C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 836902 | |||||||
chr7:837033 | G | A | 1 | a0003c0003t0001g0277 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.78-1765G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837033 | |||||||
chr7:837041 | T | C | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.78-1757T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837041 | |||||||
chr7:837256 | T | C | 1 | a0002c0005t0001g0027 | 2 | HG02071.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.78-1542T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837256 | |||||||
chr7:837275 | G | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78-1523G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837275 | |||||||
chr7:837342 | G | A | 1 | a0003c0003t0001g0278 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.78-1456G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837342 | |||||||
chr7:837437 | TCAATTTT others(16): Show |
T | 1 | a0002c0002t0009g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.78-1357_78-1335del others(23): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | INFO_REALIGN_3_PRIME | chr7 | 837437 | ||||||
chr7:837444 | T | C | 59 | a0001c0001t0001g0279 a0003c0003t0001g0017 a0003c0003t0001g0037 others(56): Show |
62 | HG00323.hp2 HG00558.hp2 HG00621.hp2 others(59): Show |
intron_variant | MODIFIER | c.78-1354T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837444 | |||||||
chr7:837474 | A | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-1324A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837474 | |||||||
chr7:837501 | A | T | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.78-1297A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837501 | |||||||
chr7:837519 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-1279A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837519 | |||||||
chr7:837638 | A | G | 1 | a0002c0002t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.78-1160A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837638 | |||||||
chr7:837848 | A | G | 2 | a0002c0002t0001g0024 a0002c0002t0001g0061 |
3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78-950A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837848 | |||||||
chr7:837885 | C | G | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.78-913C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 837885 | |||||||
chr7:838178 | T | A | 32 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(29): Show |
36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.78-620T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838178 | |||||||
chr7:838206 | C | G | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.78-592C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838206 | |||||||
chr7:838212 | C | G | 2 | a0002c0002t0001g0015 a0002c0002t0001g0259 |
4 | HG02258.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.78-586C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838212 | |||||||
chr7:838394 | A | C | 5 | a0002c0005t0001g0009 a0002c0005t0001g0052 a0002c0005t0001g0053 others(2): Show |
7 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.78-404A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838394 | |||||||
chr7:838401 | G | A | 1 | a0012c0030t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.78-397G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838401 | |||||||
chr7:838431 | G | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.78-367G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838431 | |||||||
chr7:838483 | G | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.78-315G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838483 | |||||||
chr7:838624 | A | G | 2 | a0002c0002t0001g0024 a0002c0002t0001g0061 |
3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.78-174A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838624 | |||||||
chr7:838652 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.78-146G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838652 | |||||||
chr7:838795 | T | C | 9 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 others(6): Show |
9 | HG02040.hp1 HG02698.hp1 NA18944.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.78-3T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 1/18 | chr7 | 838795 | |||||||
chr7:839109 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+123G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839109 | |||||||
chr7:839130 | T | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.266+144T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839130 | |||||||
chr7:839161 | G | A | 1 | a0001c0006t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266+175G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839161 | |||||||
chr7:839341 | A | C | 2 | a0001c0006t0018g0260 a0012c0030t0001g0051 |
2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.266+355A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839341 | |||||||
chr7:839366 | G | A | 1 | a0004c0007t0004g0120 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.266+380G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839366 | |||||||
chr7:839436 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.266+450A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839436 | |||||||
chr7:839478 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+492G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839478 | |||||||
chr7:839515 | AGCTGGGA others(296): Show |
A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(170): Show |
208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.266+534_266+836del | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 839515 | ||||||
chr7:839558 | C | CT | 6 | a0001c0006t0018g0260 a0002c0002t0001g0002 a0002c0002t0001g0047 others(3): Show |
7 | HG02027.hp1 HG02132.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.266+581dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 839558 | ||||||
chr7:839585 | C | T | 1 | a0003c0003t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.266+599C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839585 | |||||||
chr7:839601 | G | T | 2 | a0003c0003t0001g0307 a0003c0003t0001g0308 |
2 | NA18968.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.266+615G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839601 | |||||||
chr7:839664 | T | C | 65 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(62): Show |
68 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.266+678T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839664 | |||||||
chr7:839744 | G | A | 1 | a0003c0003t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.266+758G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839744 | |||||||
chr7:839899 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.266+913C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839899 | |||||||
chr7:839936 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(170): Show |
208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.266+950G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839936 | |||||||
chr7:839957 | T | C | 1 | a0001c0004t0002g0216 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.266+971T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839957 | |||||||
chr7:839977 | A | G | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.266+991A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 839977 | |||||||
chr7:840137 | T | C | 2 | a0001c0006t0001g0054 a0001c0006t0001g0055 |
2 | HG02970.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.266+1151T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840137 | |||||||
chr7:840262 | G | A | 1 | a0001c0001t0021g0121 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.266+1276G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840262 | |||||||
chr7:840270 | G | A | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.266+1284G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840270 | |||||||
chr7:840306 | C | A | 1 | a0003c0003t0001g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.266+1320C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840306 | |||||||
chr7:840358 | C | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.266+1372C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840358 | |||||||
chr7:840426 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.266+1440G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840426 | |||||||
chr7:840535 | C | G | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.267-1411C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840535 | |||||||
chr7:840574 | T | G | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.267-1372T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840574 | |||||||
chr7:840583 | T | G | 1 | a0001c0001t0001g0122 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.267-1363T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840583 | |||||||
chr7:840639 | C | CT | 98 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(95): Show |
107 | HG00323.hp2 HG00544.hp2 HG00621.hp1 others(104): Show |
intron_variant | MODIFIER | c.267-1287dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | ||||||
chr7:840639 | C | CTT | 46 | a0001c0001t0016g0264 a0001c0004t0002g0242 a0001c0004t0002g0243 others(43): Show |
64 | HG00558.hp1 HG00558.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.267-1288_267-1287d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | ||||||
chr7:840639 | CT | C | 6 | a0002c0002t0001g0032 a0002c0002t0001g0245 a0002c0002t0001g0268 others(3): Show |
7 | HG00140.hp2 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.267-1287delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | ||||||
chr7:840639 | CTTTTT | C | 136 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(133): Show |
166 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.267-1291_267-1287d others(7): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840639 | ||||||
chr7:840694 | T | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(171): Show |
209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.267-1252T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840694 | |||||||
chr7:840766 | C | T | 4 | a0001c0001t0001g0199 a0002c0002t0001g0064 a0002c0002t0003g0022 others(1): Show |
5 | NA18944.hp2 NA18967.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.267-1180C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840766 | |||||||
chr7:840861 | C | T | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.267-1085C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840861 | |||||||
chr7:840912 | A | T | 1 | a0002c0002t0001g0257 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.267-1034A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840912 | |||||||
chr7:840986 | T | G | 58 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(55): Show |
61 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.267-960T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 840986 | |||||||
chr7:840994 | C | CG | 32 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(29): Show |
36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.267-951dupG | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 840994 | ||||||
chr7:841011 | G | A | 1 | a0002c0002t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.267-935G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841011 | |||||||
chr7:841133 | A | G | 7 | a0001c0001t0001g0108 a0001c0001t0001g0193 a0001c0001t0001g0194 others(4): Show |
7 | HG00408.hp2 HG02015.hp2 NA18943.hp1 others(4): Show |
intron_variant | MODIFIER | c.267-813A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841133 | |||||||
chr7:841143 | G | A | 2 | a0002c0005t0001g0086 a0002c0005t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.267-803G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841143 | |||||||
chr7:841161 | G | A | 1 | a0007c0010t0001g0201 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.267-785G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841161 | |||||||
chr7:841219 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.267-727C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841219 | |||||||
chr7:841244 | A | AT | 139 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(136): Show |
168 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.267-685dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 841244 | ||||||
chr7:841244 | A | ATT | 37 | a0001c0001t0001g0189 a0001c0001t0001g0202 a0001c0004t0002g0013 others(34): Show |
44 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(41): Show |
intron_variant | MODIFIER | c.267-686_267-685dup others(2): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 841244 | ||||||
chr7:841244 | A | ATTT | 64 | a0001c0001t0001g0190 a0001c0001t0001g0191 a0003c0003t0001g0017 others(61): Show |
67 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(64): Show |
intron_variant | MODIFIER | c.267-687_267-685dup others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | INFO_REALIGN_3_PRIME | chr7 | 841244 | ||||||
chr7:841346 | C | G | 65 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(62): Show |
68 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.267-600C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841346 | |||||||
chr7:841366 | C | T | 1 | a0003c0003t0001g0329 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.267-580C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841366 | |||||||
chr7:841444 | G | A | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.267-502G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841444 | |||||||
chr7:841537 | T | G | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.267-409T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841537 | |||||||
chr7:841643 | G | T | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(315): Show |
389 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(386): Show |
intron_variant | MODIFIER | c.267-303G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841643 | |||||||
chr7:841752 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0103 a0001c0001t0001g0104 |
4 | HG01106.hp2 HG01433.hp1 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-194G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841752 | |||||||
chr7:841858 | C | G | 1 | a0001c0001t0001g0198 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.267-88C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841858 | |||||||
chr7:841884 | A | G | 1 | a0002c0002t0001g0081 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.267-62A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 2/18 | chr7 | 841884 | |||||||
chr7:842207 | G | T | 1 | a0003c0003t0001g0327 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.451+77G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842207 | |||||||
chr7:842221 | C | T | 172 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(169): Show |
206 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.451+91C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842221 | |||||||
chr7:842327 | A | T | 30 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(27): Show |
34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.451+197A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842327 | |||||||
chr7:842398 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.451+268G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842398 | |||||||
chr7:842575 | G | T | 4 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.451+445G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842575 | |||||||
chr7:842581 | G | T | 1 | a0001c0001t0001g0041 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.451+451G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842581 | |||||||
chr7:842613 | G | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0128 a0001c0001t0001g0129 others(4): Show |
7 | HG00738.hp2 HG00741.hp1 HG00741.hp2 others(4): Show |
intron_variant | MODIFIER | c.451+483G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842613 | |||||||
chr7:842710 | G | A | 7 | a0002c0002t0001g0033 a0002c0002t0001g0246 a0002c0002t0001g0247 others(4): Show |
8 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.452-496G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842710 | |||||||
chr7:842810 | G | C | 1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.452-396G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842810 | |||||||
chr7:842906 | G | A | 59 | a0002c0002t0001g0251 a0003c0003t0001g0017 a0003c0003t0001g0037 others(56): Show |
62 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.452-300G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842906 | |||||||
chr7:842989 | G | A | 1 | a0002c0002t0001g0333 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.452-217G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 842989 | |||||||
chr7:843122 | T | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.452-84T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 843122 | |||||||
chr7:843191 | TG | T | 32 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(29): Show |
36 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(33): Show |
intron_variant | MODIFIER | c.452-14delG | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 843191 | |||||||
chr7:843192 | GT | G | 101 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0263 others(98): Show |
121 | HG00140.hp1 HG00323.hp2 HG00558.hp2 others(118): Show |
splice_region_variant&intron_variant | LOW | c.452-3delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | INFO_REALIGN_3_PRIME | chr7 | 843192 | ||||||
chr7:843194 | T | G | 4 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0007c0010t0001g0132 others(1): Show |
4 | NA18963.hp2 NA18968.hp1 NA18977.hp2 others(1): Show |
intron_variant | MODIFIER | c.452-12T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 3/18 | chr7 | 843194 | |||||||
chr7:843255 | C | G | 4 | a0003c0003t0001g0323 a0003c0003t0001g0324 a0003c0003t0010g0325 others(1): Show |
4 | HG00323.hp2 HG00642.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.478+23C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 4/18 | chr7 | 843255 | |||||||
chr7:843258 | C | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(172): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.478+26C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 4/18 | chr7 | 843258 | |||||||
chr7:843641 | A | G | 7 | a0003c0003t0001g0318 a0003c0003t0001g0319 a0003c0003t0001g0320 others(4): Show |
7 | HG02602.hp2 HG02735.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+121A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843641 | |||||||
chr7:843685 | C | A | 3 | a0008c0011t0006g0269 a0008c0011t0006g0271 a0016c0018t0006g0270 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.658+165C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843685 | |||||||
chr7:843697 | T | A | 5 | a0001c0001t0001g0202 a0001c0004t0002g0222 a0001c0004t0002g0223 others(2): Show |
5 | NA19006.hp1 NA19006.hp2 NA19062.hp1 others(2): Show |
intron_variant | MODIFIER | c.658+177T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843697 | |||||||
chr7:843706 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.658+186T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843706 | |||||||
chr7:843865 | G | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+345G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843865 | |||||||
chr7:843943 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.658+423G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 843943 | |||||||
chr7:844060 | C | T | 2 | a0008c0011t0006g0269 a0008c0011t0006g0271 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.658+540C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844060 | |||||||
chr7:844062 | C | T | 4 | a0001c0001t0001g0041 a0001c0001t0001g0263 a0001c0006t0018g0260 others(1): Show |
4 | HG01496.hp2 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.658+542C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844062 | |||||||
chr7:844123 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.658+603G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844123 | |||||||
chr7:844306 | C | G | 31 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.658+786C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844306 | |||||||
chr7:844333 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.658+813C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844333 | |||||||
chr7:844404 | G | A | 3 | a0002c0005t0001g0088 a0002c0005t0001g0089 a0002c0005t0001g0090 |
3 | HG02602.hp1 HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.658+884G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844404 | |||||||
chr7:844420 | G | A | 23 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0033 others(20): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.658+900G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844420 | |||||||
chr7:844517 | G | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+997G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844517 | |||||||
chr7:844580 | C | T | 4 | a0006c0009t0001g0018 a0006c0009t0001g0099 a0006c0009t0001g0100 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.658+1060C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844580 | |||||||
chr7:844642 | G | A | 57 | a0001c0001t0001g0136 a0003c0003t0001g0017 a0003c0003t0001g0037 others(54): Show |
60 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.658+1122G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844642 | |||||||
chr7:844668 | G | A | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.658+1148G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844668 | |||||||
chr7:844685 | T | A | 2 | a0002c0002t0001g0015 a0002c0002t0001g0259 |
4 | HG02258.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.658+1165T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844685 | |||||||
chr7:844810 | G | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+1290G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844810 | |||||||
chr7:844925 | C | A | 1 | a0003c0003t0001g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.658+1405C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844925 | |||||||
chr7:844938 | G | A | 1 | a0002c0002t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.658+1418G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844938 | |||||||
chr7:844961 | G | A | 1 | a0003c0003t0001g0283 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.658+1441G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 844961 | |||||||
chr7:845028 | A | G | 122 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(119): Show |
144 | HG00140.hp1 HG00323.hp2 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.658+1508A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845028 | |||||||
chr7:845067 | A | G | 146 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(143): Show |
179 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(176): Show |
intron_variant | MODIFIER | c.658+1547A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845067 | |||||||
chr7:845092 | T | C | 1 | a0001c0025t0001g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.658+1572T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845092 | |||||||
chr7:845106 | C | T | 144 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(141): Show |
176 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.658+1586C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845106 | |||||||
chr7:845149 | T | G | 1 | a0002c0005t0001g0053 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.658+1629T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845149 | |||||||
chr7:845178 | A | G | 2 | a0002c0002t0001g0024 a0002c0002t0001g0061 |
3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.658+1658A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845178 | |||||||
chr7:845306 | G | A | 2 | a0002c0002t0001g0033 a0002c0002t0001g0246 |
3 | HG02451.hp2 HG02486.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.658+1786G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845306 | |||||||
chr7:845332 | T | G | 3 | a0002c0002t0001g0020 a0002c0002t0001g0067 a0002c0002t0001g0068 |
4 | NA18946.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.658+1812T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845332 | |||||||
chr7:845364 | C | G | 1 | a0005c0008t0001g0036 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.658+1844C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845364 | |||||||
chr7:845402 | C | G | 2 | a0002c0005t0001g0097 a0002c0005t0001g0098 |
2 | HG04115.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.658+1882C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845402 | |||||||
chr7:845444 | T | C | 1 | a0005c0008t0001g0036 | 2 | HG01884.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.658+1924T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845444 | |||||||
chr7:845765 | A | G | 40 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(37): Show |
57 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(54): Show |
intron_variant | MODIFIER | c.658+2245A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845765 | |||||||
chr7:845907 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.658+2387G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845907 | |||||||
chr7:845926 | C | T | 2 | a0001c0006t0018g0260 a0012c0030t0001g0051 |
2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.658+2406C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845926 | |||||||
chr7:845947 | G | A | 1 | a0001c0006t0012g0043 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.658+2427G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845947 | |||||||
chr7:845960 | G | C | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.658+2440G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 845960 | |||||||
chr7:846059 | A | G | 17 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0033 others(14): Show |
29 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.658+2539A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846059 | |||||||
chr7:846202 | G | A | 1 | a0003c0003t0005g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.658+2682G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846202 | |||||||
chr7:846211 | C | T | 1 | a0004c0007t0004g0187 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.658+2691C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846211 | |||||||
chr7:846253 | C | T | 65 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(62): Show |
68 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.658+2733C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846253 | |||||||
chr7:846265 | T | C | 1 | a0003c0003t0001g0284 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.658+2745T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846265 | |||||||
chr7:846289 | C | A | 261 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(258): Show |
313 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(310): Show |
intron_variant | MODIFIER | c.658+2769C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846289 | |||||||
chr7:846527 | A | T | 30 | a0001c0001t0001g0202 a0001c0004t0002g0013 a0001c0004t0002g0014 others(27): Show |
34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.658+3007A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846527 | |||||||
chr7:846602 | C | T | 22 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.658+3082C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846602 | |||||||
chr7:846746 | A | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(196): Show |
248 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.658+3226A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846746 | |||||||
chr7:846905 | T | C | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.658+3385T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846905 | |||||||
chr7:846930 | C | T | 1 | a0001c0025t0001g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.658+3410C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846930 | |||||||
chr7:846962 | A | G | 4 | a0001c0001t0001g0007 a0001c0001t0001g0183 a0001c0001t0001g0184 others(1): Show |
8 | HG01256.hp2 HG01258.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.658+3442A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 846962 | |||||||
chr7:847004 | T | TAAAAAAA others(3): Show |
1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3492_658+3493i others(12): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847004 | ||||||
chr7:847013 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3493T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847013 | |||||||
chr7:847014 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3494T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847014 | |||||||
chr7:847015 | A | T | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.658+3495A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847015 | |||||||
chr7:847020 | T | A | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.658+3500T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847020 | |||||||
chr7:847206 | G | A | 1 | a0002c0002t0001g0069 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.658+3686G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847206 | |||||||
chr7:847215 | G | T | 7 | a0001c0001t0001g0137 a0001c0001t0001g0179 a0001c0001t0001g0180 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.658+3695G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847215 | |||||||
chr7:847254 | G | A | 1 | a0001c0006t0012g0044 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.658+3734G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847254 | |||||||
chr7:847255 | G | GTCCCCTG others(137): Show |
1 | a0003c0003t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.658+3759_658+3902d others(146): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847255 | ||||||
chr7:847282 | G | A | 24 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(21): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.658+3762G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847282 | |||||||
chr7:847351 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.658+3831G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847351 | |||||||
chr7:847373 | G | T | 2 | a0008c0011t0006g0269 a0008c0011t0006g0271 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.658+3853G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847373 | |||||||
chr7:847382 | G | A | 2 | a0003c0003t0001g0284 a0003c0003t0001g0285 |
2 | HG01123.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.658+3862G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847382 | |||||||
chr7:847396 | G | A | 56 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(53): Show |
59 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.658+3876G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847396 | |||||||
chr7:847423 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.658+3903A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847423 | |||||||
chr7:847483 | T | C | 2 | a0002c0005t0001g0086 a0002c0005t0001g0087 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.659-3901T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847483 | |||||||
chr7:847489 | C | T | 1 | a0004c0007t0001g0178 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.659-3895C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847489 | |||||||
chr7:847490 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(172): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.659-3894A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847490 | |||||||
chr7:847517 | GGCCTTCC others(79): Show |
G | 3 | a0001c0001t0001g0177 a0001c0006t0012g0043 a0001c0006t0012g0044 |
3 | HG01243.hp2 HG02717.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.659-3781_659-3696d others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847517 | ||||||
chr7:847541 | C | A | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.659-3843C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847541 | |||||||
chr7:847544 | T | C | 1 | a0021c0029t0001g0141 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.659-3840T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847544 | |||||||
chr7:847573 | C | T | 3 | a0001c0004t0002g0013 a0001c0004t0002g0233 a0020c0014t0002g0239 |
3 | NA18612.hp1 NA18939.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.659-3811C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847573 | |||||||
chr7:847603 | A | G | 96 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0107 others(93): Show |
115 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.659-3781A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847603 | |||||||
chr7:847625 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.659-3759C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847625 | |||||||
chr7:847681 | G | A | 2 | a0001c0001t0001g0041 a0001c0001t0001g0263 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.659-3703G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847681 | |||||||
chr7:847686 | G | A | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3698G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847686 | |||||||
chr7:847712 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.659-3672G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847712 | |||||||
chr7:847739 | G | A | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-3645G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847739 | |||||||
chr7:847748 | G | A | 227 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(224): Show |
291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.659-3636G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847748 | |||||||
chr7:847748 | G | GCAGCGCC others(79): Show |
1 | a0012c0030t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.659-3551_659-3550i others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847748 | ||||||
chr7:847766 | G | A | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3618G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847766 | |||||||
chr7:847766 | G | GGAGTTGG others(79): Show |
57 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(54): Show |
60 | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.659-3551_659-3550i others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847766 | ||||||
chr7:847766 | G | GGAGTTGG others(79): Show |
1 | a0003c0003t0001g0317 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.659-3533_659-3532i others(88): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847766 | ||||||
chr7:847834 | G | A | 8 | a0001c0006t0001g0019 a0001c0006t0001g0054 a0001c0006t0001g0055 others(5): Show |
9 | HG01515.hp1 HG01517.hp1 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.659-3550G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847834 | |||||||
chr7:847841 | C | T | 1 | a0003c0003t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.659-3543C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847841 | |||||||
chr7:847845 | C | T | 5 | a0002c0002t0001g0032 a0002c0002t0001g0034 a0002c0002t0001g0245 others(2): Show |
7 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3539C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847845 | |||||||
chr7:847852 | G | A | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-3532G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847852 | |||||||
chr7:847859 | G | A | 175 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(172): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.659-3525G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847859 | |||||||
chr7:847861 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.659-3523G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847861 | |||||||
chr7:847874 | G | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(21): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.659-3510G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847874 | |||||||
chr7:847884 | G | C | 1 | a0021c0029t0001g0141 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.659-3500G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847884 | |||||||
chr7:847933 | C | T | 5 | a0003c0003t0001g0017 a0003c0003t0001g0314 a0003c0003t0001g0315 others(2): Show |
7 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.659-3451C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847933 | |||||||
chr7:847934 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.659-3450G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847934 | |||||||
chr7:847976 | T | TCCTGGGG others(29): Show |
12 | a0001c0006t0001g0019 a0001c0006t0001g0045 a0001c0006t0001g0046 others(9): Show |
13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.659-3393_659-3358d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 847976 | ||||||
chr7:847991 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(128): Show |
159 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.659-3393C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 847991 | |||||||
chr7:848012 | C | G | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.659-3372C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848012 | |||||||
chr7:848017 | G | A | 5 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(2): Show |
5 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.659-3367G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848017 | |||||||
chr7:848064 | G | A | 3 | a0002c0005t0001g0088 a0002c0005t0001g0089 a0002c0005t0001g0090 |
3 | HG02602.hp1 HG02698.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.659-3320G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848064 | |||||||
chr7:848068 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.659-3316C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848068 | |||||||
chr7:848069 | G | A | 1 | a0001c0004t0023g0241 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.659-3315G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848069 | |||||||
chr7:848074 | C | G | 1 | a0001c0001t0001g0208 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.659-3310C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848074 | |||||||
chr7:848084 | T | TCCTGGGG others(29): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.659-3285_659-3284i others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 848084 | ||||||
chr7:848084 | T | TCCTGGGG others(29): Show |
137 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(134): Show |
168 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.659-3279_659-3244d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 848084 | ||||||
chr7:848135 | C | T | 1 | a0002c0002t0009g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.659-3249C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848135 | |||||||
chr7:848185 | C | A | 1 | a0002c0002t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.659-3199C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848185 | |||||||
chr7:848198 | G | GA | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.659-3186_659-3185i others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848198 | |||||||
chr7:848360 | A | G | 1 | a0001c0006t0001g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.659-3024A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848360 | |||||||
chr7:848368 | G | C | 1 | a0001c0001t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.659-3016G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848368 | |||||||
chr7:848559 | A | G | 5 | a0002c0002t0001g0032 a0002c0002t0001g0034 a0002c0002t0001g0245 others(2): Show |
7 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-2825A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848559 | |||||||
chr7:848653 | A | T | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.659-2731A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848653 | |||||||
chr7:848739 | C | G | 3 | a0003c0003t0007g0311 a0003c0003t0007g0312 a0003c0003t0007g0313 |
3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.659-2645C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848739 | |||||||
chr7:848799 | C | G | 2 | a0001c0001t0001g0105 a0001c0001t0001g0106 |
2 | HG01261.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.659-2585C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848799 | |||||||
chr7:848811 | T | C | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.659-2573T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848811 | |||||||
chr7:848855 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.659-2529T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848855 | |||||||
chr7:848973 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.659-2411C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848973 | |||||||
chr7:848973 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.659-2411C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 848973 | |||||||
chr7:849003 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.659-2381G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849003 | |||||||
chr7:849028 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.659-2356C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849028 | |||||||
chr7:849077 | A | G | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(315): Show |
389 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(386): Show |
intron_variant | MODIFIER | c.659-2307A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849077 | |||||||
chr7:849113 | G | A | 1 | a0001c0004t0002g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.659-2271G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849113 | |||||||
chr7:849180 | A | G | 1 | a0001c0004t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.659-2204A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849180 | |||||||
chr7:849197 | C | T | 2 | a0008c0011t0006g0269 a0008c0011t0006g0271 |
2 | HG02723.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.659-2187C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849197 | |||||||
chr7:849245 | C | T | 1 | a0001c0004t0002g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.659-2139C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849245 | |||||||
chr7:849246 | G | A | 142 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(139): Show |
173 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.659-2138G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849246 | |||||||
chr7:849248 | C | A | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.659-2136C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849248 | |||||||
chr7:849282 | G | A | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.659-2102G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849282 | |||||||
chr7:849334 | G | A | 2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.659-2050G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849334 | |||||||
chr7:849389 | A | G | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.659-1995A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849389 | |||||||
chr7:849532 | A | G | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.659-1852A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849532 | |||||||
chr7:849672 | A | T | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.659-1712A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849672 | |||||||
chr7:849696 | C | T | 1 | a0001c0001t0001g0139 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.659-1688C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849696 | |||||||
chr7:849721 | T | C | 43 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(40): Show |
46 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(43): Show |
intron_variant | MODIFIER | c.659-1663T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849721 | |||||||
chr7:849955 | G | A | 1 | a0001c0001t0001g0206 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.659-1429G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 849955 | |||||||
chr7:850049 | G | A | 1 | a0002c0002t0001g0070 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.659-1335G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850049 | |||||||
chr7:850174 | A | G | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.659-1210A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850174 | |||||||
chr7:850221 | C | T | 49 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0030 others(46): Show |
60 | HG00323.hp1 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.659-1163C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850221 | |||||||
chr7:850255 | G | A | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.659-1129G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850255 | |||||||
chr7:850279 | GCCTCCA | G | 12 | a0001c0006t0001g0019 a0001c0006t0001g0045 a0001c0006t0001g0046 others(9): Show |
13 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(10): Show |
intron_variant | MODIFIER | c.659-1098_659-1093d others(8): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850279 | ||||||
chr7:850356 | AC | A | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.659-1025delC | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850356 | ||||||
chr7:850414 | T | C | 199 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(196): Show |
248 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.659-970T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850414 | |||||||
chr7:850456 | C | T | 7 | a0002c0002t0001g0033 a0002c0002t0001g0246 a0002c0002t0001g0247 others(4): Show |
8 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.659-928C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850456 | |||||||
chr7:850647 | T | C | 172 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(169): Show |
207 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(204): Show |
intron_variant | MODIFIER | c.659-737T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850647 | |||||||
chr7:850767 | T | TA | 22 | a0002c0002t0001g0047 a0002c0002t0001g0061 a0002c0002t0001g0063 others(19): Show |
25 | HG00140.hp2 HG00558.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.659-602dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | ||||||
chr7:850767 | T | TAA | 41 | a0001c0001t0001g0041 a0001c0001t0001g0263 a0001c0001t0001g0265 others(38): Show |
48 | HG00544.hp2 HG01243.hp1 HG01243.hp2 others(45): Show |
intron_variant | MODIFIER | c.659-603_659-602dup others(2): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | ||||||
chr7:850767 | T | TAAA | 8 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0191 others(5): Show |
8 | HG00621.hp1 HG01070.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.659-604_659-602dup others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | ||||||
chr7:850767 | T | TAAAA | 110 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(107): Show |
138 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.659-605_659-602dup others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | ||||||
chr7:850767 | T | TAAAAA | 12 | a0001c0001t0001g0026 a0001c0001t0001g0140 a0001c0001t0001g0143 others(9): Show |
12 | HG00544.hp1 HG00673.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.659-606_659-602dup others(5): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | INFO_REALIGN_3_PRIME | chr7 | 850767 | ||||||
chr7:850782 | A | C | 2 | a0003c0003t0005g0272 a0003c0003t0005g0273 |
2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.659-602A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850782 | |||||||
chr7:850782 | AC | A | 24 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(21): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.659-601delC | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850782 | |||||||
chr7:850783 | C | A | 21 | a0001c0001t0001g0028 a0001c0001t0001g0204 a0001c0001t0001g0265 others(18): Show |
24 | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.659-601C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850783 | |||||||
chr7:850864 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.659-520G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850864 | |||||||
chr7:850959 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.659-425A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850959 | |||||||
chr7:850980 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.659-404A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 850980 | |||||||
chr7:851009 | A | C | 1 | a0001c0004t0002g0238 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.659-375A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851009 | |||||||
chr7:851055 | G | A | 7 | a0002c0002t0001g0033 a0002c0002t0001g0246 a0002c0002t0001g0247 others(4): Show |
8 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.659-329G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851055 | |||||||
chr7:851069 | A | G | 1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.659-315A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851069 | |||||||
chr7:851276 | C | T | 11 | a0003c0003t0001g0280 a0003c0003t0001g0282 a0003c0003t0001g0302 others(8): Show |
11 | HG02056.hp2 HG02074.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.659-108C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851276 | |||||||
chr7:851341 | T | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(171): Show |
209 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.659-43T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 5/18 | chr7 | 851341 | |||||||
chr7:851547 | C | CGAT | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(262): Show |
317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.757+66_757+68dupGA others(1): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | INFO_REALIGN_3_PRIME | chr7 | 851547 | ||||||
chr7:851701 | G | A | 44 | a0001c0001t0001g0041 a0001c0001t0001g0108 a0001c0001t0001g0202 others(41): Show |
51 | HG00544.hp2 HG00621.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.757+219G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | chr7 | 851701 | |||||||
chr7:851841 | C | T | 3 | a0008c0011t0006g0269 a0008c0011t0006g0271 a0016c0018t0006g0270 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.758-109C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | chr7 | 851841 | |||||||
chr7:851946 | G | A | 1 | a0002c0002t0003g0085 | 1 | NA18944.hp2 | splice_region_variant&intron_variant | LOW | c.758-4G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 6/18 | chr7 | 851946 | |||||||
chr7:852109 | C | T | 1 | a0001c0004t0002g0243 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.851+66C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 7/18 | chr7 | 852109 | |||||||
chr7:852143 | T | C | 1 | a0003c0003t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.851+100T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 7/18 | chr7 | 852143 | |||||||
chr7:852409 | G | T | 2 | a0003c0003t0001g0321 a0003c0003t0001g0322 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.852-200G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 7/18 | chr7 | 852409 | |||||||
chr7:852699 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.910+32G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852699 | |||||||
chr7:852706 | C | G | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.910+39C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852706 | |||||||
chr7:852707 | G | T | 3 | a0003c0003t0007g0311 a0003c0003t0007g0312 a0003c0003t0007g0313 |
3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.910+40G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852707 | |||||||
chr7:852770 | G | A | 1 | a0002c0002t0001g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.911-40G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852770 | |||||||
chr7:852779 | C | A | 4 | a0001c0006t0001g0019 a0001c0006t0001g0054 a0001c0006t0001g0055 others(1): Show |
5 | HG02965.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.911-31C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 8/18 | chr7 | 852779 | |||||||
chr7:853002 | C | A | 1 | a0003c0003t0001g0314 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1053+50C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853002 | |||||||
chr7:853144 | A | G | 41 | a0001c0004t0002g0237 a0002c0002t0001g0002 a0002c0002t0001g0010 others(38): Show |
58 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(55): Show |
intron_variant | MODIFIER | c.1053+192A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853144 | |||||||
chr7:853252 | A | G | 4 | a0001c0006t0001g0019 a0001c0006t0001g0054 a0001c0006t0001g0055 others(1): Show |
5 | HG02965.hp2 HG02970.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1054-157A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853252 | |||||||
chr7:853265 | C | T | 63 | a0001c0001t0001g0175 a0002c0002t0009g0040 a0003c0003t0001g0017 others(60): Show |
66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1054-144C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853265 | |||||||
chr7:853268 | C | T | 1 | a0001c0004t0002g0236 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1054-141C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 9/18 | chr7 | 853268 | |||||||
chr7:853660 | G | C | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(170): Show |
208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1263+42G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853660 | |||||||
chr7:853687 | T | C | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1263+69T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853687 | |||||||
chr7:853770 | G | A | 128 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(125): Show |
156 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.1263+152G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853770 | |||||||
chr7:853828 | G | A | 1 | a0002c0002t0001g0247 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1263+210G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853828 | |||||||
chr7:853879 | C | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1263+261C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853879 | |||||||
chr7:853880 | A | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.1263+262A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853880 | |||||||
chr7:853960 | T | C | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1263+342T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 853960 | |||||||
chr7:854000 | G | A | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(315): Show |
389 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(386): Show |
intron_variant | MODIFIER | c.1263+382G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854000 | |||||||
chr7:854018 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0263 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1263+400C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854018 | |||||||
chr7:854062 | G | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1263+444G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854062 | |||||||
chr7:854169 | T | G | 1 | a0002c0005t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1263+551T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854169 | |||||||
chr7:854259 | G | A | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1263+641G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854259 | |||||||
chr7:854301 | G | A | 1 | a0001c0001t0017g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1264-619G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854301 | |||||||
chr7:854315 | G | A | 22 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1264-605G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854315 | |||||||
chr7:854343 | T | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1264-577T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854343 | |||||||
chr7:854390 | G | A | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1264-530G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854390 | |||||||
chr7:854443 | C | A | 1 | a0001c0001t0001g0142 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1264-477C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854443 | |||||||
chr7:854534 | C | T | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1264-386C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854534 | |||||||
chr7:854551 | C | T | 2 | a0001c0001t0001g0158 a0001c0001t0001g0159 |
2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1264-369C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854551 | |||||||
chr7:854714 | A | AAT | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1264-196_1264-195d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 854714 | ||||||
chr7:854734 | C | T | 1 | a0002c0005t0001g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1264-186C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854734 | |||||||
chr7:854785 | T | C | 24 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(21): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1264-135T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854785 | |||||||
chr7:854822 | G | GATTGTCG others(15): Show |
1 | a0002c0002t0001g0084 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1264-96_1264-75dup others(22): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | INFO_REALIGN_3_PRIME | chr7 | 854822 | ||||||
chr7:854876 | G | A | 1 | a0002c0002t0001g0065 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1264-44G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854876 | |||||||
chr7:854897 | G | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0131 |
2 | HG02109.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1264-23G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854897 | |||||||
chr7:854914 | C | A | 1 | a0003c0003t0001g0293 | 1 | HG03017.hp2 | splice_region_variant&intron_variant | LOW | c.1264-6C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 10/18 | chr7 | 854914 | |||||||
chr7:855021 | C | G | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1350+15C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855021 | |||||||
chr7:855027 | G | A | 1 | a0002c0002t0009g0039 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1350+21G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855027 | |||||||
chr7:855035 | A | T | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1350+29A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855035 | |||||||
chr7:855039 | T | A | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1350+33T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855039 | |||||||
chr7:855040 | A | T | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1350+34A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855040 | |||||||
chr7:855096 | T | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1350+90T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855096 | |||||||
chr7:855163 | G | T | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1350+157G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855163 | |||||||
chr7:855165 | G | A | 1 | a0001c0004t0002g0216 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1350+159G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855165 | |||||||
chr7:855193 | T | C | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1350+187T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855193 | |||||||
chr7:855204 | C | T | 141 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(138): Show |
172 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1350+198C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855204 | |||||||
chr7:855250 | A | C | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1350+244A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855250 | |||||||
chr7:855261 | C | T | 2 | a0002c0002t0001g0024 a0002c0002t0001g0061 |
3 | HG00639.hp1 HG01099.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1350+255C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855261 | |||||||
chr7:855300 | T | C | 1 | a0001c0001t0001g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1350+294T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855300 | |||||||
chr7:855305 | G | A | 1 | a0002c0005t0001g0088 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1350+299G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855305 | |||||||
chr7:855357 | G | A | 1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1350+351G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855357 | |||||||
chr7:855389 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1350+383C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855389 | |||||||
chr7:855463 | C | T | 1 | a0001c0006t0001g0056 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1350+457C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855463 | |||||||
chr7:855485 | G | A | 1 | a0003c0003t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1350+479G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855485 | |||||||
chr7:855648 | G | A | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
123 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1350+642G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855648 | |||||||
chr7:855746 | C | T | 1 | a0002c0005t0001g0095 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1351-612C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855746 | |||||||
chr7:855787 | T | G | 1 | a0002c0002t0001g0253 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1351-571T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855787 | |||||||
chr7:855807 | A | G | 57 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(54): Show |
60 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.1351-551A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855807 | |||||||
chr7:855824 | T | G | 5 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0174 others(2): Show |
5 | NA18963.hp2 NA18968.hp1 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.1351-534T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855824 | |||||||
chr7:855837 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1351-521G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855837 | |||||||
chr7:855868 | G | C | 35 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(32): Show |
51 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(48): Show |
intron_variant | MODIFIER | c.1351-490G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855868 | |||||||
chr7:855900 | C | T | 4 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1351-458C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855900 | |||||||
chr7:855925 | G | A | 1 | a0002c0002t0001g0067 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1351-433G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855925 | |||||||
chr7:855964 | C | T | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1351-394C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 855964 | |||||||
chr7:856171 | C | T | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1351-187C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 856171 | |||||||
chr7:856291 | A | G | 22 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1351-67A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 11/18 | chr7 | 856291 | |||||||
chr7:856440 | G | C | 1 | a0003c0003t0001g0276 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1394+39G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856440 | |||||||
chr7:856448 | G | A | 1 | a0013c0020t0001g0252 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1394+47G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856448 | |||||||
chr7:856505 | C | T | 22 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1394+104C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856505 | |||||||
chr7:856537 | C | T | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1394+136C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856537 | |||||||
chr7:856561 | G | A | 2 | a0009c0013t0001g0124 a0009c0013t0001g0163 |
2 | NA18951.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1394+160G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856561 | |||||||
chr7:856606 | G | A | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1394+205G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856606 | |||||||
chr7:856649 | G | T | 1 | a0002c0002t0001g0256 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1394+248G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856649 | |||||||
chr7:856656 | T | C | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1394+255T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856656 | |||||||
chr7:856657 | G | C | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1394+256G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856657 | |||||||
chr7:856671 | G | C | 3 | a0001c0001t0001g0143 a0001c0001t0001g0177 a0001c0001t0001g0215 |
3 | NA18939.hp1 NA18998.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1394+270G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856671 | |||||||
chr7:856749 | G | A | 4 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0263 others(1): Show |
4 | HG02647.hp1 HG02647.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1394+348G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856749 | |||||||
chr7:856808 | G | A | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(170): Show |
208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1394+407G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856808 | |||||||
chr7:856816 | C | G | 1 | a0003c0003t0001g0310 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1394+415C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856816 | |||||||
chr7:856888 | G | A | 1 | a0003c0003t0001g0310 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1394+487G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856888 | |||||||
chr7:856923 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1394+522G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856923 | |||||||
chr7:856947 | T | G | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1394+546T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856947 | |||||||
chr7:856966 | C | T | 5 | a0002c0002t0001g0033 a0002c0002t0001g0247 a0002c0002t0001g0249 others(2): Show |
6 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1394+565C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856966 | |||||||
chr7:856983 | C | G | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1394+582C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 856983 | |||||||
chr7:857010 | A | G | 1 | a0002c0005t0001g0090 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1394+609A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857010 | |||||||
chr7:857014 | A | C | 262 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(259): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.1394+613A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857014 | |||||||
chr7:857015 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1394+614G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857015 | |||||||
chr7:857015 | G | C | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1394+614G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857015 | |||||||
chr7:857038 | A | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.1394+637A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857038 | |||||||
chr7:857061 | G | T | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1394+660G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857061 | |||||||
chr7:857105 | GTCTT | G | 3 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0113 |
3 | NA18957.hp1 NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1394+709_1394+712d others(6): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | INFO_REALIGN_3_PRIME | chr7 | 857105 | ||||||
chr7:857129 | C | A | 1 | a0002c0002t0001g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1395-699C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857129 | |||||||
chr7:857137 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1395-691G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857137 | |||||||
chr7:857338 | T | G | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1395-490T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857338 | |||||||
chr7:857360 | T | G | 1 | a0002c0002t0001g0072 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1395-468T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857360 | |||||||
chr7:857504 | A | C | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1395-324A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857504 | |||||||
chr7:857736 | G | A | 30 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(27): Show |
34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1395-92G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 12/18 | chr7 | 857736 | |||||||
chr7:858074 | C | T | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1524+117C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858074 | |||||||
chr7:858113 | C | T | 1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1524+156C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858113 | |||||||
chr7:858147 | C | T | 26 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(23): Show |
42 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.1524+190C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858147 | |||||||
chr7:858158 | G | A | 6 | a0002c0002t0001g0033 a0002c0002t0001g0246 a0002c0002t0001g0247 others(3): Show |
7 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1524+201G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858158 | |||||||
chr7:858180 | G | C | 1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1524+223G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858180 | |||||||
chr7:858195 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1524+238C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858195 | |||||||
chr7:858210 | A | G | 65 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(62): Show |
68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+253A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858210 | |||||||
chr7:858283 | G | T | 1 | a0002c0002t0001g0251 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1524+326G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858283 | |||||||
chr7:858365 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1524+408G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858365 | |||||||
chr7:858390 | CT | C | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
291 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1524+446delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 858390 | ||||||
chr7:858390 | CTT | C | 20 | a0003c0003t0001g0280 a0003c0003t0001g0281 a0003c0003t0001g0282 others(17): Show |
20 | HG01106.hp1 HG02056.hp2 HG02074.hp2 others(17): Show |
intron_variant | MODIFIER | c.1524+445_1524+446d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 858390 | ||||||
chr7:858500 | G | A | 3 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 |
3 | HG02015.hp2 NA18943.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.1524+543G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858500 | |||||||
chr7:858526 | C | T | 1 | a0003c0003t0001g0310 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1524+569C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858526 | |||||||
chr7:858555 | A | G | 1 | a0002c0005t0001g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1524+598A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858555 | |||||||
chr7:858753 | A | G | 1 | a0002c0002t0001g0079 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1524+796A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858753 | |||||||
chr7:858789 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1524+832G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858789 | |||||||
chr7:858868 | C | T | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1524+911C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858868 | |||||||
chr7:858871 | T | C | 65 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(62): Show |
68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+914T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858871 | |||||||
chr7:858875 | C | T | 2 | a0001c0004t0002g0234 a0001c0004t0023g0241 |
2 | NA18978.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.1524+918C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858875 | |||||||
chr7:858919 | C | T | 1 | a0018c0017t0001g0309 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1524+962C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858919 | |||||||
chr7:858928 | C | T | 65 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(62): Show |
68 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(65): Show |
intron_variant | MODIFIER | c.1524+971C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858928 | |||||||
chr7:858983 | G | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1524+1026G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 858983 | |||||||
chr7:859010 | G | A | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1524+1053G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859010 | |||||||
chr7:859018 | T | G | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1524+1061T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859018 | |||||||
chr7:859107 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1525-1021C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859107 | |||||||
chr7:859108 | G | A | 9 | a0001c0001t0001g0011 a0001c0001t0001g0028 a0001c0001t0001g0138 others(6): Show |
12 | HG00423.hp1 HG00673.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.1525-1020G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859108 | |||||||
chr7:859152 | C | CA | 13 | a0001c0001t0001g0103 a0001c0001t0001g0130 a0001c0001t0001g0165 others(10): Show |
14 | HG02257.hp2 HG02559.hp1 HG02738.hp1 others(11): Show |
intron_variant | MODIFIER | c.1525-960dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 859152 | ||||||
chr7:859152 | CA | C | 7 | a0001c0001t0001g0172 a0001c0022t0001g0156 a0002c0002t0001g0259 others(4): Show |
7 | HG01109.hp2 HG01975.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1525-960delA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 859152 | ||||||
chr7:859265 | C | CACGAGG | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.1525-858_1525-853d others(8): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | INFO_REALIGN_3_PRIME | chr7 | 859265 | ||||||
chr7:859289 | C | T | 24 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(21): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1525-839C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859289 | |||||||
chr7:859309 | T | C | 1 | a0001c0006t0001g0054 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1525-819T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859309 | |||||||
chr7:859418 | G | A | 2 | a0003c0003t0001g0294 a0003c0003t0001g0295 |
2 | NA19055.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1525-710G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859418 | |||||||
chr7:859478 | C | T | 1 | a0001c0001t0001g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1525-650C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859478 | |||||||
chr7:859603 | G | A | 1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1525-525G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859603 | |||||||
chr7:859727 | A | G | 1 | a0001c0006t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1525-401A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859727 | |||||||
chr7:859806 | C | T | 173 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(170): Show |
208 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.1525-322C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859806 | |||||||
chr7:859826 | G | C | 3 | a0008c0011t0006g0269 a0008c0011t0006g0271 a0016c0018t0006g0270 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1525-302G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859826 | |||||||
chr7:859844 | G | A | 1 | a0003c0003t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1525-284G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859844 | |||||||
chr7:859850 | G | A | 1 | a0001c0006t0001g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1525-278G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859850 | |||||||
chr7:859909 | G | A | 1 | a0002c0005t0001g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1525-219G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859909 | |||||||
chr7:859950 | A | G | 239 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(236): Show |
277 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(274): Show |
intron_variant | MODIFIER | c.1525-178A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 859950 | |||||||
chr7:860073 | A | C | 174 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(171): Show |
210 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1525-55A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 13/18 | chr7 | 860073 | |||||||
chr7:860398 | G | A | 24 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(21): Show |
38 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(35): Show |
intron_variant | MODIFIER | c.1779+16G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860398 | |||||||
chr7:860528 | G | A | 7 | a0001c0006t0001g0019 a0001c0006t0001g0054 a0001c0006t0001g0055 others(4): Show |
8 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1779+146G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860528 | |||||||
chr7:860839 | A | T | 1 | a0002c0002t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1779+457A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860839 | |||||||
chr7:860855 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1779+473G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860855 | |||||||
chr7:860941 | C | G | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1780-439C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860941 | |||||||
chr7:860947 | C | A | 1 | a0001c0001t0001g0209 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1780-433C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 860947 | |||||||
chr7:861049 | G | A | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1780-331G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861049 | |||||||
chr7:861051 | A | T | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1780-329A>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861051 | |||||||
chr7:861109 | T | G | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1780-271T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861109 | |||||||
chr7:861172 | C | T | 39 | a0002c0002t0001g0002 a0002c0002t0001g0010 a0002c0002t0001g0020 others(36): Show |
56 | HG00558.hp1 HG02015.hp1 HG02027.hp1 others(53): Show |
intron_variant | MODIFIER | c.1780-208C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861172 | |||||||
chr7:861212 | C | T | 1 | a0010c0026t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1780-168C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861212 | |||||||
chr7:861268 | C | G | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1780-112C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861268 | |||||||
chr7:861322 | C | T | 3 | a0003c0003t0001g0284 a0003c0003t0001g0285 a0003c0021t0020g0300 |
3 | HG01123.hp2 HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1780-58C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861322 | |||||||
chr7:861341 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1780-39G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 14/18 | chr7 | 861341 | |||||||
chr7:861633 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1864+169G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861633 | |||||||
chr7:861642 | T | C | 1 | a0012c0030t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1864+178T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861642 | |||||||
chr7:861745 | C | T | 22 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1864+281C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861745 | |||||||
chr7:861746 | T | C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0011 others(69): Show |
90 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1864+282T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861746 | |||||||
chr7:861937 | C | T | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1864+473C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861937 | |||||||
chr7:861998 | C | T | 1 | a0002c0002t0009g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1864+534C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861998 | |||||||
chr7:861999 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0001g0183 a0002c0002t0001g0024 others(1): Show |
9 | HG00639.hp1 HG01099.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.1864+535G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 861999 | |||||||
chr7:862089 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1864+625C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862089 | |||||||
chr7:862117 | C | T | 4 | a0006c0009t0001g0018 a0006c0009t0001g0099 a0006c0009t0001g0100 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1864+653C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862117 | |||||||
chr7:862138 | C | T | 3 | a0003c0003t0007g0311 a0003c0003t0007g0312 a0003c0003t0007g0313 |
3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1864+674C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862138 | |||||||
chr7:862156 | A | G | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1864+692A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862156 | |||||||
chr7:862339 | A | G | 1 | a0002c0002t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1864+875A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862339 | |||||||
chr7:862398 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1864+934C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862398 | |||||||
chr7:862445 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1864+981C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862445 | |||||||
chr7:862542 | A | C | 1 | a0001c0004t0002g0240 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1864+1078A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862542 | |||||||
chr7:862718 | T | A | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1864+1254T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862718 | |||||||
chr7:862722 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1864+1258G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862722 | |||||||
chr7:862757 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1864+1293A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862757 | |||||||
chr7:862771 | T | A | 1 | a0001c0006t0001g0055 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1864+1307T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862771 | |||||||
chr7:862813 | C | G | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1864+1349C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862813 | |||||||
chr7:862874 | G | A | 2 | a0001c0001t0001g0261 a0001c0001t0001g0265 |
2 | HG02647.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1864+1410G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862874 | |||||||
chr7:862878 | G | A | 2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1864+1414G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862878 | |||||||
chr7:862890 | G | A | 1 | a0001c0006t0001g0102 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1864+1426G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862890 | |||||||
chr7:862912 | G | A | 1 | a0002c0002t0001g0068 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1864+1448G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862912 | |||||||
chr7:862933 | C | G | 1 | a0003c0003t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1864+1469C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862933 | |||||||
chr7:862947 | C | G | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1864+1483C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862947 | |||||||
chr7:862950 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
174 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1864+1486G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 862950 | |||||||
chr7:863108 | C | G | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1864+1644C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863108 | |||||||
chr7:863123 | C | A | 3 | a0008c0011t0006g0269 a0008c0011t0006g0271 a0016c0018t0006g0270 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1864+1659C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863123 | |||||||
chr7:863129 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(129): Show |
160 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1864+1665G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863129 | |||||||
chr7:863235 | C | T | 1 | a0001c0004t0002g0218 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1864+1771C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863235 | |||||||
chr7:863252 | A | ATTCACCA others(53): Show |
94 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(91): Show |
119 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.1864+1829_1864+183 others(64): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863252 | ||||||
chr7:863252 | A | ATTCACCA others(113): Show |
63 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(60): Show |
66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1864+1906_1864+190 others(124): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863252 | ||||||
chr7:863290 | G | A | 22 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1864+1826G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863290 | |||||||
chr7:863294 | T | G | 130 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(127): Show |
158 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1864+1830T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863294 | |||||||
chr7:863342 | G | GCCCTCCC others(113): Show |
2 | a0008c0011t0006g0271 a0016c0018t0006g0270 |
2 | HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1864+1906_1864+190 others(124): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863342 | ||||||
chr7:863342 | G | GCCCTCCC others(113): Show |
1 | a0008c0011t0006g0269 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1864+1906_1864+190 others(124): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 863342 | ||||||
chr7:863513 | A | G | 1 | a0001c0001t0017g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1864+2049A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863513 | |||||||
chr7:863550 | C | T | 1 | a0006c0009t0001g0101 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1864+2086C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863550 | |||||||
chr7:863648 | C | A | 11 | a0001c0006t0001g0019 a0001c0006t0001g0045 a0001c0006t0001g0046 others(8): Show |
12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1864+2184C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863648 | |||||||
chr7:863660 | C | A | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1864+2196C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863660 | |||||||
chr7:863754 | C | T | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1865-2198C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863754 | |||||||
chr7:863785 | A | G | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1865-2167A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863785 | |||||||
chr7:863955 | G | C | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1865-1997G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 863955 | |||||||
chr7:864001 | C | A | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1865-1951C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864001 | |||||||
chr7:864065 | T | C | 1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1865-1887T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864065 | |||||||
chr7:864125 | A | G | 1 | a0017c0027t0001g0059 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1865-1827A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864125 | |||||||
chr7:864266 | G | A | 4 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1865-1686G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864266 | |||||||
chr7:864318 | C | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(140): Show |
174 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(171): Show |
intron_variant | MODIFIER | c.1865-1634C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864318 | |||||||
chr7:864336 | T | C | 1 | a0002c0005t0001g0097 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1865-1616T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864336 | |||||||
chr7:864340 | G | A | 5 | a0001c0001t0001g0114 a0003c0003t0001g0323 a0003c0003t0001g0324 others(2): Show |
5 | HG00323.hp2 HG00642.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.1865-1612G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864340 | |||||||
chr7:864411 | G | A | 1 | a0016c0018t0006g0270 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1865-1541G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864411 | |||||||
chr7:864490 | G | A | 3 | a0002c0005t0001g0009 a0002c0005t0001g0052 a0002c0005t0001g0053 |
5 | HG00140.hp2 HG01255.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.1865-1462G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864490 | |||||||
chr7:864509 | G | A | 1 | a0003c0003t0005g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1865-1443G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864509 | |||||||
chr7:864514 | A | G | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1865-1438A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864514 | |||||||
chr7:864554 | C | CA | 87 | a0001c0001t0001g0030 a0001c0001t0001g0041 a0001c0001t0001g0148 others(84): Show |
104 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.1865-1379dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | ||||||
chr7:864554 | C | CAAA | 28 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(25): Show |
32 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1865-1381_1865-137 others(7): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | ||||||
chr7:864554 | CA | C | 9 | a0001c0001t0001g0137 a0001c0001t0001g0171 a0002c0002t0001g0077 others(6): Show |
12 | HG01167.hp1 HG01243.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1865-1379delA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | ||||||
chr7:864554 | CAAAAA | C | 28 | a0001c0001t0001g0008 a0001c0001t0001g0110 a0001c0001t0001g0112 others(25): Show |
31 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.1865-1383_1865-137 others(9): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864554 | ||||||
chr7:864573 | A | G | 5 | a0002c0002t0001g0010 a0002c0002t0001g0064 a0002c0002t0001g0066 others(2): Show |
7 | HG02015.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1865-1379A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864573 | |||||||
chr7:864620 | A | G | 1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1865-1332A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864620 | |||||||
chr7:864647 | GACAAAGA others(29): Show |
G | 1 | a0002c0002t0001g0069 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1865-1303_1865-126 others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864647 | ||||||
chr7:864668 | G | A | 2 | a0001c0001t0001g0005 a0001c0001t0001g0168 |
3 | HG02155.hp2 HG03654.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.1865-1284G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864668 | |||||||
chr7:864693 | ATCTCGGC others(49): Show |
A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(206): Show |
243 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.1865-1253_1865-119 others(60): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | INFO_REALIGN_3_PRIME | chr7 | 864693 | ||||||
chr7:864770 | A | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0263 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1865-1182A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864770 | |||||||
chr7:864778 | G | A | 30 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(27): Show |
34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1865-1174G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864778 | |||||||
chr7:864789 | C | T | 34 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(31): Show |
38 | HG00544.hp2 HG00621.hp1 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.1865-1163C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864789 | |||||||
chr7:864942 | C | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.1865-1010C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864942 | |||||||
chr7:864982 | A | C | 1 | a0001c0004t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1865-970A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 864982 | |||||||
chr7:865005 | C | A | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1865-947C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865005 | |||||||
chr7:865120 | G | T | 98 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(95): Show |
123 | HG00099.hp1 HG00323.hp1 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.1865-832G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865120 | |||||||
chr7:865177 | A | G | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1865-775A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865177 | |||||||
chr7:865356 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.1865-596C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865356 | |||||||
chr7:865592 | C | T | 20 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(17): Show |
34 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1865-360C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865592 | |||||||
chr7:865593 | G | A | 1 | a0003c0003t0001g0293 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1865-359G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865593 | |||||||
chr7:865628 | T | C | 149 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(146): Show |
180 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1865-324T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865628 | |||||||
chr7:865736 | C | T | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1865-216C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865736 | |||||||
chr7:865781 | T | C | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1865-171T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865781 | |||||||
chr7:865920 | G | A | 1 | a0001c0006t0001g0045 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1865-32G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 15/18 | chr7 | 865920 | |||||||
chr7:866081 | G | A | 1 | a0001c0025t0001g0200 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1980+14G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866081 | |||||||
chr7:866107 | A | G | 1 | a0012c0030t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1980+40A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866107 | |||||||
chr7:866118 | T | C | 3 | a0002c0002t0001g0032 a0002c0002t0001g0245 a0002c0002t0001g0268 |
4 | HG02723.hp1 HG02886.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+51T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866118 | |||||||
chr7:866149 | A | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1980+82A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866149 | |||||||
chr7:866159 | G | A | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1980+92G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866159 | |||||||
chr7:866185 | G | C | 3 | a0001c0001t0001g0208 a0001c0001t0011g0167 a0001c0001t0011g0335 |
3 | HG00323.hp1 HG00642.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1980+118G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866185 | |||||||
chr7:866227 | G | C | 63 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(60): Show |
66 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(63): Show |
intron_variant | MODIFIER | c.1980+160G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866227 | |||||||
chr7:866249 | G | A | 1 | a0001c0004t0002g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1980+182G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866249 | |||||||
chr7:866333 | T | C | 4 | a0006c0009t0001g0018 a0006c0009t0001g0099 a0006c0009t0001g0100 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1980+266T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866333 | |||||||
chr7:866399 | G | A | 1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1980+332G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866399 | |||||||
chr7:866440 | C | T | 1 | a0003c0003t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1980+373C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866440 | |||||||
chr7:866523 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1980+456C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866523 | |||||||
chr7:866532 | T | G | 4 | a0001c0001t0001g0025 a0001c0001t0001g0161 a0001c0001t0001g0168 others(1): Show |
5 | HG01433.hp1 HG01517.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1980+465T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866532 | |||||||
chr7:866532 | T | TCCCCCAC others(29): Show |
10 | a0003c0003t0001g0298 a0003c0003t0001g0299 a0003c0003t0001g0330 others(7): Show |
10 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.1980+493_1980+494i others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866532 | ||||||
chr7:866561 | T | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1980+494T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866561 | |||||||
chr7:866562 | A | ACCTTCGC others(29): Show |
8 | a0002c0002t0001g0078 a0002c0002t0003g0006 a0002c0002t0003g0022 others(5): Show |
14 | HG02071.hp1 HG02622.hp2 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.1980+599_1980+634d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866562 | ||||||
chr7:866562 | A | ACCTTCGC others(65): Show |
8 | a0002c0002t0001g0033 a0002c0002t0001g0038 a0002c0002t0001g0246 others(5): Show |
9 | HG01081.hp1 HG02451.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980+563_1980+634d others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866562 | ||||||
chr7:866562 | A | G | 240 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(237): Show |
278 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(275): Show |
intron_variant | MODIFIER | c.1980+495A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866562 | |||||||
chr7:866593 | C | CCCGGGCC others(101): Show |
1 | a0001c0001t0001g0155 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1980+562_1980+563i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866593 | ||||||
chr7:866630 | C | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0168 |
2 | HG03654.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1980+563C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866630 | |||||||
chr7:866631 | C | CGGGCCTT others(101): Show |
11 | a0001c0006t0001g0019 a0001c0006t0001g0045 a0001c0006t0001g0046 others(8): Show |
12 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(9): Show |
intron_variant | MODIFIER | c.1980+634_1980+635i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866631 | ||||||
chr7:866631 | C | CGGGCCTT others(101): Show |
1 | a0001c0001t0001g0210 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866631 | ||||||
chr7:866631 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0168 |
2 | HG03654.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.1980+564C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866631 | |||||||
chr7:866649 | G | C | 1 | a0001c0001t0001g0031 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1980+582G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866649 | |||||||
chr7:866665 | C | CGTGGGCC others(63): Show |
3 | a0002c0002t0001g0020 a0002c0002t0001g0067 a0002c0002t0001g0068 |
4 | NA18946.hp1 NA18964.hp2 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+598_1980+599i others(72): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866665 | |||||||
chr7:866665 | C | CGTGGGCC others(63): Show |
1 | a0001c0001t0001g0106 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1980+598_1980+599i others(72): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866665 | |||||||
chr7:866666 | C | G | 13 | a0001c0001t0001g0136 a0001c0001t0001g0155 a0001c0001t0001g0161 others(10): Show |
13 | HG00673.hp2 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1980+599C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866666 | |||||||
chr7:866667 | C | CGGGCCTT others(245): Show |
1 | a0003c0003t0001g0280 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1980+634_1980+635i others(254): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGGGCCTT others(137): Show |
3 | a0003c0003t0010g0325 a0003c0003t0010g0326 a0003c0021t0020g0300 |
3 | HG00323.hp2 HG00642.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1980+634_1980+635i others(146): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGGGCCTT others(101): Show |
2 | a0003c0003t0001g0321 a0003c0003t0001g0322 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1980+634_1980+635i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGGGCCTT others(65): Show |
47 | a0001c0006t0018g0260 a0002c0002t0001g0074 a0002c0002t0001g0081 others(44): Show |
50 | HG00558.hp2 HG00639.hp2 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.1980+634_1980+635i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGGGCCTT others(101): Show |
1 | a0010c0026t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1980+634_1980+635i others(110): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGGGCCTT others(29): Show |
18 | a0001c0004t0002g0013 a0001c0004t0002g0217 a0001c0004t0002g0218 others(15): Show |
20 | HG01243.hp2 HG02132.hp2 HG02717.hp1 others(17): Show |
intron_variant | MODIFIER | c.1980+615_1980+650d others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGGGCCTT others(65): Show |
7 | a0001c0001t0001g0041 a0001c0001t0001g0105 a0001c0001t0001g0123 others(4): Show |
7 | HG01975.hp2 HG02273.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | CGT | 4 | a0001c0001t0001g0106 a0002c0002t0001g0020 a0002c0002t0001g0067 others(1): Show |
5 | HG01261.hp1 NA18946.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.1980+601_1980+602i others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866667 | ||||||
chr7:866667 | C | T | 13 | a0001c0001t0001g0136 a0001c0001t0001g0155 a0001c0001t0001g0161 others(10): Show |
13 | HG00673.hp2 HG02040.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.1980+600C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866667 | |||||||
chr7:866668 | G | GGGCCTTC others(65): Show |
1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1980+650_1980+651i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866668 | ||||||
chr7:866678 | CCCCACTG others(27): Show |
C | 1 | a0002c0002t0001g0077 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1980+615_1980+648d others(36): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866678 | ||||||
chr7:866702 | G | A | 4 | a0001c0001t0001g0136 a0001c0001t0001g0155 a0001c0001t0001g0161 others(1): Show |
4 | HG03471.hp2 HG03654.hp2 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+635G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866702 | |||||||
chr7:866702 | G | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0108 a0001c0001t0001g0153 others(5): Show |
8 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1980+635G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866702 | |||||||
chr7:866702 | G | GTGGGCCT others(65): Show |
6 | a0001c0001t0001g0007 a0001c0001t0001g0183 a0002c0002t0009g0039 others(3): Show |
7 | HG01256.hp2 HG01884.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(74): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866702 | ||||||
chr7:866703 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0108 a0001c0001t0001g0153 others(5): Show |
8 | HG01361.hp2 HG01515.hp1 HG01517.hp1 others(5): Show |
intron_variant | MODIFIER | c.1980+636T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866703 | |||||||
chr7:866712 | G | GC | 82 | a0001c0001t0001g0041 a0001c0001t0001g0106 a0001c0001t0001g0135 others(79): Show |
88 | HG00140.hp2 HG00408.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.1980+655dupC | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCC | 44 | a0001c0001t0001g0123 a0001c0001t0001g0155 a0001c0001t0001g0166 others(41): Show |
51 | HG00544.hp1 HG01496.hp2 HG01891.hp1 others(48): Show |
intron_variant | MODIFIER | c.1980+654_1980+655d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(30): Show |
8 | a0001c0001t0001g0008 a0001c0001t0001g0111 a0001c0001t0001g0112 others(5): Show |
9 | HG00673.hp2 HG01167.hp2 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(39): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(31): Show |
21 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0008 others(18): Show |
22 | HG00408.hp1 HG00621.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(67): Show |
1 | a0001c0001t0001g0031 | 2 | HG02055.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(76): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(103): Show |
2 | a0001c0001t0001g0127 a0001c0001t0001g0153 |
2 | HG01361.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(112): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(29): Show |
1 | a0001c0001t0001g0211 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(38): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(30): Show |
22 | a0001c0001t0001g0261 a0001c0001t0021g0121 a0001c0004t0002g0014 others(19): Show |
24 | HG00544.hp2 HG00621.hp1 HG01981.hp1 others(21): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(39): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(31): Show |
6 | a0001c0004t0022g0221 a0002c0002t0001g0024 a0002c0002t0001g0032 others(3): Show |
7 | HG00639.hp1 HG01099.hp1 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(32): Show |
2 | a0002c0002t0001g0015 a0002c0002t0001g0259 |
4 | HG02258.hp2 HG02818.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(41): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(66): Show |
34 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0011 others(31): Show |
39 | HG00099.hp1 HG00323.hp1 HG01071.hp1 others(36): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(75): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(67): Show |
46 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0011 others(43): Show |
55 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(52): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(76): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(68): Show |
1 | a0001c0001t0001g0026 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(77): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(174): Show |
1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(183): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(319): Show |
1 | a0001c0001t0001g0005 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1980+650_1980+651i others(328): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(66): Show |
3 | a0002c0002t0001g0001 a0002c0002t0001g0035 a0002c0002t0001g0253 |
7 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(75): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(67): Show |
4 | a0002c0002t0001g0001 a0002c0002t0001g0035 a0002c0002t0001g0255 others(1): Show |
7 | HG01081.hp2 HG01175.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(76): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(102): Show |
5 | a0001c0001t0001g0003 a0001c0001t0001g0030 a0001c0001t0001g0108 others(2): Show |
6 | HG03017.hp1 HG03490.hp2 HG03710.hp1 others(3): Show |
intron_variant | MODIFIER | c.1980+650_1980+651i others(111): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(103): Show |
3 | a0001c0001t0001g0003 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG03927.hp2 HG03942.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(112): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(138): Show |
1 | a0001c0001t0001g0126 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(147): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(139): Show |
2 | a0001c0001t0001g0125 a0004c0007t0004g0146 |
2 | HG04199.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1980+650_1980+651i others(148): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(234): Show |
1 | a0003c0003t0001g0323 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(243): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(233): Show |
1 | a0003c0003t0001g0324 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1980+650_1980+651i others(242): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCAC others(173): Show |
1 | a0001c0001t0001g0157 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1980+650_1980+651i others(182): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866712 | G | GCCCCCCC others(569): Show |
1 | a0001c0022t0001g0156 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1980+655_1980+656i others(578): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 866712 | ||||||
chr7:866723 | G | A | 1 | a0001c0004t0002g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.1980+656G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866723 | |||||||
chr7:866723 | G | C | 1 | a0003c0003t0001g0303 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1980+656G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866723 | |||||||
chr7:866729 | C | T | 1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1980+662C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866729 | |||||||
chr7:866730 | G | A | 4 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 others(1): Show |
8 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1980+663G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866730 | |||||||
chr7:866771 | G | A | 2 | a0009c0013t0001g0124 a0009c0013t0001g0163 |
2 | NA18951.hp2 NA19057.hp2 |
intron_variant | MODIFIER | c.1980+704G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866771 | |||||||
chr7:866991 | A | G | 318 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(315): Show |
389 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(386): Show |
intron_variant | MODIFIER | c.1980+924A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 866991 | |||||||
chr7:867013 | G | T | 28 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(25): Show |
32 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1980+946G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867013 | |||||||
chr7:867036 | C | G | 1 | a0001c0001t0001g0184 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1980+969C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867036 | |||||||
chr7:867102 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(245): Show |
287 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(284): Show |
intron_variant | MODIFIER | c.1980+1035A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867102 | |||||||
chr7:867113 | G | A | 1 | a0002c0002t0003g0073 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1980+1046G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867113 | |||||||
chr7:867143 | G | A | 3 | a0006c0009t0001g0018 a0006c0009t0001g0100 a0006c0009t0001g0101 |
4 | HG02622.hp2 HG02630.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.1980+1076G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867143 | |||||||
chr7:867155 | C | T | 1 | a0003c0003t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1980+1088C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867155 | |||||||
chr7:867200 | G | A | 30 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(27): Show |
34 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1980+1133G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867200 | |||||||
chr7:867346 | C | T | 2 | a0001c0006t0018g0260 a0012c0030t0001g0051 |
2 | HG01496.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.1980+1279C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867346 | |||||||
chr7:867367 | G | A | 1 | a0010c0026t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1980+1300G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867367 | |||||||
chr7:867390 | T | C | 1 | a0001c0001t0024g0212 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1980+1323T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867390 | |||||||
chr7:867510 | G | T | 1 | a0001c0001t0001g0133 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1980+1443G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867510 | |||||||
chr7:867733 | C | A | 1 | a0002c0002t0001g0245 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1981-1616C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867733 | |||||||
chr7:867755 | A | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1981-1594A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867755 | |||||||
chr7:867762 | G | A | 4 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-1587G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867762 | |||||||
chr7:867778 | C | T | 1 | a0001c0001t0001g0126 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1981-1571C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867778 | |||||||
chr7:867812 | G | A | 1 | a0001c0004t0002g0232 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1981-1537G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867812 | |||||||
chr7:867916 | C | T | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1981-1433C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867916 | |||||||
chr7:867943 | G | C | 1 | a0001c0004t0002g0237 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1981-1406G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867943 | |||||||
chr7:867951 | G | A | 1 | a0002c0002t0009g0040 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1981-1398G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 867951 | |||||||
chr7:868035 | C | G | 1 | a0001c0001t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1981-1314C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868035 | |||||||
chr7:868035 | C | T | 4 | a0006c0009t0001g0018 a0006c0009t0001g0099 a0006c0009t0001g0100 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981-1314C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868035 | |||||||
chr7:868109 | C | T | 1 | a0003c0003t0001g0330 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1981-1240C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868109 | |||||||
chr7:868128 | G | A | 1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1981-1221G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868128 | |||||||
chr7:868158 | T | G | 1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1981-1191T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868158 | |||||||
chr7:868193 | C | T | 2 | a0003c0003t0001g0289 a0003c0003t0001g0290 |
2 | NA18978.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.1981-1156C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868193 | |||||||
chr7:868195 | T | C | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.1981-1154T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868195 | |||||||
chr7:868272 | G | A | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1981-1077G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868272 | |||||||
chr7:868373 | C | T | 1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1981-976C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868373 | |||||||
chr7:868374 | G | A | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.1981-975G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868374 | |||||||
chr7:868461 | C | T | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1981-888C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868461 | |||||||
chr7:868466 | G | A | 3 | a0005c0008t0001g0016 a0005c0008t0001g0036 a0005c0008t0001g0266 |
6 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1981-883G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868466 | |||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1981-742_1981-741i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
3 | a0008c0011t0006g0269 a0008c0011t0006g0271 a0016c0018t0006g0270 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1981-738_1981-737i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(257): Show |
1 | a0001c0001t0001g0166 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1981-720_1981-719i others(266): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
2 | a0001c0001t0001g0125 a0001c0001t0001g0126 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
1 | a0001c0001t0001g0279 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
106 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(103): Show |
132 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(335): Show |
1 | a0004c0007t0004g0187 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1981-667_1981-666i others(344): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
5 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(2): Show |
5 | HG02886.hp1 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981-699_1981-698i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(260): Show |
1 | a0001c0001t0001g0193 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1981-736_1981-735i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
2 | a0001c0001t0001g0190 a0001c0001t0001g0191 |
2 | HG02622.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1981-756_1981-755i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(221): Show |
1 | a0001c0004t0002g0229 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1981-819_1981-818i others(230): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(221): Show |
28 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(25): Show |
32 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1981-819_1981-818i others(230): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(223): Show |
1 | a0019c0015t0008g0235 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1981-850_1981-849i others(232): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | A | ATGTTGGT others(259): Show |
1 | a0001c0001t0001g0202 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1981-856_1981-855i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868480 | ATGTTGGT others(31): Show |
A | 1 | a0002c0002t0001g0024 | 2 | HG00639.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.1981-818_1981-781d others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868480 | ||||||
chr7:868492 | T | TGGGGGGG others(260): Show |
1 | a0001c0001t0017g0162 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1981-667_1981-666i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868492 | ||||||
chr7:868530 | T | TGGGGGGG others(260): Show |
1 | a0001c0001t0001g0185 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1981-812_1981-811i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868530 | ||||||
chr7:868531 | G | C | 5 | a0002c0002t0001g0010 a0002c0002t0001g0064 a0002c0002t0001g0066 others(2): Show |
7 | HG02015.hp1 HG02071.hp1 HG02129.hp2 others(4): Show |
intron_variant | MODIFIER | c.1981-818G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868531 | |||||||
chr7:868531 | G | GGGGGGGC others(221): Show |
2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(230): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868531 | ||||||
chr7:868531 | G | T | 2 | a0001c0004t0002g0224 a0002c0002t0001g0061 |
2 | HG03209.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.1981-818G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868531 | |||||||
chr7:868538 | C | CAGTGCTG others(259): Show |
2 | a0001c0001t0001g0169 a0001c0001t0001g0175 |
2 | HG01978.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868538 | ||||||
chr7:868568 | T | TGGGGGGG others(220): Show |
1 | a0001c0004t0002g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1981-781_1981-780i others(229): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868568 | |||||||
chr7:868569 | T | TGGGGGGC others(525): Show |
3 | a0003c0003t0001g0017 a0003c0003t0001g0316 a0003c0003t0001g0327 |
5 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(2): Show |
intron_variant | MODIFIER | c.1981-705_1981-704i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | ||||||
chr7:868569 | T | TGGGGGGC others(525): Show |
1 | a0003c0003t0001g0314 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1981-705_1981-704i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | ||||||
chr7:868569 | T | TGGGGGGC others(107): Show |
2 | a0001c0001t0001g0011 a0001c0001t0001g0160 |
4 | HG00423.hp1 NA18947.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-667_1981-666i others(116): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | ||||||
chr7:868569 | T | TGGGGGGC others(260): Show |
2 | a0001c0001t0001g0041 a0001c0001t0001g0263 |
2 | HG02647.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1981-667_1981-666i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | ||||||
chr7:868569 | T | TGGGGGGC others(526): Show |
1 | a0003c0003t0001g0292 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1981-736_1981-735i others(535): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | ||||||
chr7:868569 | T | TGGGGGGC others(526): Show |
1 | a0003c0003t0001g0283 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1981-736_1981-735i others(535): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868569 | ||||||
chr7:868570 | G | T | 1 | a0001c0004t0002g0224 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1981-779G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868570 | |||||||
chr7:868602 | C | CGGATGGG others(259): Show |
1 | a0001c0001t0001g0214 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868602 | ||||||
chr7:868607 | G | T | 1 | a0001c0004t0002g0229 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1981-742G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868607 | |||||||
chr7:868626 | T | C | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1981-723T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868626 | |||||||
chr7:868651 | A | ACAGTGCT others(259): Show |
4 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(1): Show |
4 | HG01106.hp1 HG02615.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868651 | ||||||
chr7:868651 | A | G | 4 | a0001c0004t0002g0229 a0008c0011t0006g0269 a0008c0011t0006g0271 others(1): Show |
4 | HG02723.hp2 HG03098.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-698A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868651 | |||||||
chr7:868660 | G | GTTCCCTG others(260): Show |
1 | a0001c0001t0001g0261 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868660 | ||||||
chr7:868679 | G | A | 22 | a0001c0006t0018g0260 a0002c0002t0001g0001 a0002c0002t0001g0015 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1981-670G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868679 | |||||||
chr7:868682 | T | TGGGGGGC others(259): Show |
1 | a0001c0001t0001g0188 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868682 | |||||||
chr7:868682 | T | TGGGGGGG others(525): Show |
1 | a0003c0003t0001g0295 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1981-667_1981-666i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868682 | |||||||
chr7:868683 | T | G | 262 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(259): Show |
314 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(311): Show |
intron_variant | MODIFIER | c.1981-666T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868683 | |||||||
chr7:868689 | G | A | 7 | a0003c0003t0001g0017 a0003c0003t0001g0283 a0003c0003t0001g0292 others(4): Show |
9 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.1981-660G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868689 | |||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0287 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1981-629_1981-628i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
4 | a0003c0003t0001g0288 a0003c0003t0001g0296 a0003c0003t0001g0301 others(1): Show |
4 | HG01943.hp2 HG01981.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(563): Show |
1 | a0003c0003t0001g0304 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(572): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0317 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0293 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
1 | a0003c0003t0001g0321 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(639): Show |
1 | a0003c0003t0001g0281 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(648): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
2 | a0003c0003t0001g0298 a0003c0003t0001g0330 |
2 | HG03669.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
33 | a0003c0003t0001g0037 a0003c0003t0001g0276 a0003c0003t0001g0277 others(30): Show |
34 | HG00558.hp2 HG01074.hp1 HG01515.hp1 others(31): Show |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
2 | a0003c0003t0001g0284 a0003c0003t0001g0285 |
2 | HG01123.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868689 | G | GCAGTGCT others(525): Show |
1 | a0010c0026t0001g0197 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(534): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868689 | ||||||
chr7:868721 | T | C | 1 | a0012c0030t0001g0051 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1981-628T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868721 | |||||||
chr7:868721 | T | G | 1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1981-628T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868721 | |||||||
chr7:868721 | T | TGGGGGGC others(259): Show |
1 | a0005c0008t0001g0266 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1981-591_1981-590i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868721 | ||||||
chr7:868721 | T | TGGGGGGC others(259): Show |
2 | a0005c0008t0001g0016 a0005c0008t0001g0036 |
5 | HG01243.hp1 HG01884.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981-553_1981-552i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868721 | ||||||
chr7:868722 | G | GGGGGGCA others(260): Show |
1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(269): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868722 | ||||||
chr7:868727 | G | GCAGTGCT others(487): Show |
1 | a0003c0003t0001g0305 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(496): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868727 | ||||||
chr7:868727 | G | GCAGTGCT others(31): Show |
1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1981-610_1981-609i others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868727 | ||||||
chr7:868727 | G | T | 22 | a0001c0006t0018g0260 a0002c0002t0001g0001 a0002c0002t0001g0015 others(19): Show |
36 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(33): Show |
intron_variant | MODIFIER | c.1981-622G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868727 | |||||||
chr7:868760 | G | GGGGGGCA others(259): Show |
2 | a0001c0001t0001g0117 a0001c0001t0001g0118 |
2 | NA18954.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1981-553_1981-552i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868760 | ||||||
chr7:868765 | GCAGTGCT others(221): Show |
G | 5 | a0002c0002t0001g0032 a0002c0002t0001g0034 a0002c0002t0001g0245 others(2): Show |
7 | HG01891.hp1 HG02723.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1981-562_1981-335d others(2): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868765 | ||||||
chr7:868778 | C | CCTGTGGT others(373): Show |
1 | a0003c0021t0020g0300 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1981-553_1981-552i others(382): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868778 | ||||||
chr7:868781 | G | GTGGTGTT others(259): Show |
1 | a0007c0031t0014g0262 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1981-553_1981-552i others(268): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868781 | ||||||
chr7:868797 | C | G | 257 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(254): Show |
307 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(304): Show |
intron_variant | MODIFIER | c.1981-552C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868797 | |||||||
chr7:868797 | C | T | 2 | a0001c0001t0001g0138 a0001c0001t0001g0204 |
2 | HG00673.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1981-552C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868797 | |||||||
chr7:868816 | T | C | 4 | a0001c0001t0001g0138 a0001c0006t0018g0260 a0003c0003t0010g0325 others(1): Show |
4 | HG00323.hp2 HG00642.hp2 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.1981-533T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868816 | |||||||
chr7:868835 | G | T | 3 | a0001c0001t0001g0206 a0003c0003t0010g0325 a0003c0003t0010g0326 |
3 | HG00323.hp2 HG00642.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.1981-514G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868835 | |||||||
chr7:868836 | G | A | 1 | a0001c0001t0001g0213 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1981-513G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868836 | |||||||
chr7:868872 | T | TGGGGGGG others(70): Show |
1 | a0001c0001t0001g0138 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1981-458_1981-457i others(79): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868872 | ||||||
chr7:868874 | G | C | 3 | a0001c0001t0001g0172 a0002c0002t0009g0039 a0002c0002t0009g0040 |
3 | HG01975.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1981-475G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868874 | |||||||
chr7:868879 | G | GCAGTGCT others(31): Show |
1 | a0002c0002t0001g0069 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1981-372_1981-335d others(40): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868879 | ||||||
chr7:868879 | G | GCAGTGCT others(563): Show |
2 | a0003c0003t0010g0325 a0003c0003t0010g0326 |
2 | HG00323.hp2 HG00642.hp2 |
intron_variant | MODIFIER | c.1981-458_1981-457i others(572): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868879 | ||||||
chr7:868879 | GCAGTGCT others(69): Show |
G | 2 | a0001c0001t0001g0206 a0002c0002t0001g0035 |
2 | HG01978.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1981-410_1981-335d others(78): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868879 | ||||||
chr7:868892 | C | T | 256 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(253): Show |
305 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1981-457C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868892 | |||||||
chr7:868900 | G | A | 4 | a0006c0009t0001g0018 a0006c0009t0001g0099 a0006c0009t0001g0100 others(1): Show |
5 | HG02572.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1981-449G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868900 | |||||||
chr7:868912 | G | C | 16 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0033 others(13): Show |
27 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1981-437G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868912 | |||||||
chr7:868917 | A | G | 1 | a0014c0016t0001g0334 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1981-432A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868917 | |||||||
chr7:868940 | TGGTC | T | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1981-406_1981-403d others(6): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | INFO_REALIGN_3_PRIME | chr7 | 868940 | ||||||
chr7:868987 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0138 a0001c0001t0001g0160 others(2): Show |
8 | HG00423.hp1 HG00673.hp1 NA18945.hp1 others(5): Show |
intron_variant | MODIFIER | c.1981-362G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868987 | |||||||
chr7:868988 | G | C | 17 | a0001c0006t0018g0260 a0002c0002t0001g0001 a0002c0002t0001g0015 others(14): Show |
29 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1981-361G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 868988 | |||||||
chr7:869130 | G | A | 2 | a0001c0006t0001g0045 a0001c0006t0001g0056 |
2 | HG03041.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1981-219G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 869130 | |||||||
chr7:869202 | C | T | 1 | a0001c0001t0016g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1981-147C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 869202 | |||||||
chr7:869262 | T | C | 1 | a0001c0001t0001g0186 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1981-87T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 16/18 | chr7 | 869262 | |||||||
chr7:869529 | G | A | 1 | a0002c0005t0001g0023 | 2 | HG00738.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.2148+13G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869529 | |||||||
chr7:869615 | G | A | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.2148+99G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869615 | |||||||
chr7:869713 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(262): Show |
317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.2148+197T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869713 | |||||||
chr7:869818 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+302G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869818 | |||||||
chr7:869859 | C | A | 3 | a0003c0003t0007g0311 a0003c0003t0007g0312 a0003c0003t0007g0313 |
3 | HG02896.hp1 HG02897.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2148+343C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869859 | |||||||
chr7:869870 | C | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+354C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869870 | |||||||
chr7:869933 | C | T | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+417C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869933 | |||||||
chr7:869984 | G | A | 1 | a0003c0012t0005g0274 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2148+468G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 869984 | |||||||
chr7:870022 | C | T | 3 | a0008c0011t0006g0269 a0008c0011t0006g0271 a0016c0018t0006g0270 |
3 | HG02723.hp2 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2148+506C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870022 | |||||||
chr7:870040 | C | CA | 21 | a0001c0001t0001g0103 a0001c0001t0001g0150 a0001c0001t0001g0210 others(18): Show |
21 | HG01169.hp1 HG01175.hp2 HG01433.hp2 others(18): Show |
intron_variant | MODIFIER | c.2148+540dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870040 | ||||||
chr7:870153 | T | C | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2148+637T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870153 | |||||||
chr7:870196 | C | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+680C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870196 | |||||||
chr7:870205 | T | A | 1 | a0001c0004t0022g0221 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.2148+689T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870205 | |||||||
chr7:870205 | T | TA | 244 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(241): Show |
293 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(290): Show |
intron_variant | MODIFIER | c.2148+707dupA | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870205 | ||||||
chr7:870205 | T | TAA | 7 | a0001c0001t0001g0181 a0001c0001t0016g0264 a0002c0002t0001g0251 others(4): Show |
10 | HG01243.hp1 HG01884.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.2148+706_2148+707d others(4): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870205 | ||||||
chr7:870345 | T | C | 1 | a0001c0001t0001g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2148+829T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870345 | |||||||
chr7:870498 | A | C | 1 | a0001c0001t0001g0177 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2148+982A>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870498 | |||||||
chr7:870565 | A | G | 242 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(239): Show |
280 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(277): Show |
intron_variant | MODIFIER | c.2148+1049A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870565 | |||||||
chr7:870579 | C | T | 2 | a0002c0002t0009g0039 a0002c0002t0009g0040 |
2 | NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2148+1063C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870579 | |||||||
chr7:870685 | GT | G | 66 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(63): Show |
69 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.2148+1172delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870685 | ||||||
chr7:870708 | C | T | 59 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(56): Show |
62 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.2148+1192C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870708 | |||||||
chr7:870737 | CCCTGTGT others(10): Show |
C | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1225_2148+124 others(21): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870737 | ||||||
chr7:870768 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2148+1252A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870768 | |||||||
chr7:870782 | G | A | 21 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(18): Show |
35 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2148+1266G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870782 | |||||||
chr7:870802 | T | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1286T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870802 | |||||||
chr7:870808 | C | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1292C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870808 | |||||||
chr7:870810 | C | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1294C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870810 | |||||||
chr7:870810 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2148+1294C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870810 | |||||||
chr7:870813 | T | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1297T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870813 | |||||||
chr7:870823 | C | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1307C>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870823 | |||||||
chr7:870827 | A | G | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1311A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870827 | |||||||
chr7:870831 | T | G | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1315T>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870831 | |||||||
chr7:870832 | G | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1316G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870832 | |||||||
chr7:870834 | T | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1318T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870834 | |||||||
chr7:870836 | T | C | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1320T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870836 | |||||||
chr7:870841 | C | G | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1325C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870841 | |||||||
chr7:870853 | A | G | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2148+1337A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870853 | |||||||
chr7:870854 | C | G | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1338C>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870854 | |||||||
chr7:870855 | T | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1339T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870855 | |||||||
chr7:870870 | T | C | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1354T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870870 | |||||||
chr7:870873 | T | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1357T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870873 | |||||||
chr7:870875 | T | A | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1359T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870875 | |||||||
chr7:870887 | C | CT | 10 | a0001c0004t0002g0224 a0001c0004t0002g0230 a0001c0004t0022g0221 others(7): Show |
10 | HG02257.hp2 HG03209.hp2 HG03225.hp2 others(7): Show |
intron_variant | MODIFIER | c.2148+1391dupT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | ||||||
chr7:870887 | CT | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(206): Show |
248 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(245): Show |
intron_variant | MODIFIER | c.2148+1391delT | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | ||||||
chr7:870887 | CTT | C | 8 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0122 others(5): Show |
8 | HG01257.hp2 HG01975.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.2148+1390_2148+139 others(6): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | ||||||
chr7:870887 | CTTTTTTT others(5): Show |
C | 7 | a0002c0002t0001g0001 a0002c0002t0001g0035 a0002c0002t0001g0251 others(4): Show |
16 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.2148+1380_2148+139 others(16): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870887 | ||||||
chr7:870897 | T | C | 1 | a0003c0003t0001g0301 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2148+1381T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 870897 | |||||||
chr7:870973 | CTCCGCCT others(490): Show |
C | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2149-1454_2149-958 others(3): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | INFO_REALIGN_3_PRIME | chr7 | 870973 | ||||||
chr7:871038 | G | A | 6 | a0003c0003t0001g0017 a0003c0003t0001g0314 a0003c0003t0001g0316 others(3): Show |
8 | HG00639.hp2 HG00735.hp2 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.2149-1432G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871038 | |||||||
chr7:871038 | G | T | 21 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(18): Show |
35 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2149-1432G>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871038 | |||||||
chr7:871154 | G | C | 21 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(18): Show |
35 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2149-1316G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871154 | |||||||
chr7:871247 | A | G | 1 | a0002c0005t0001g0091 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2149-1223A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871247 | |||||||
chr7:871459 | T | C | 30 | a0001c0006t0012g0043 a0001c0006t0012g0044 a0002c0002t0001g0001 others(27): Show |
44 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.2149-1011T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871459 | |||||||
chr7:871473 | C | T | 133 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0263 others(130): Show |
159 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.2149-997C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871473 | |||||||
chr7:871476 | C | T | 223 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(220): Show |
276 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(273): Show |
intron_variant | MODIFIER | c.2149-994C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871476 | |||||||
chr7:871555 | C | T | 21 | a0002c0002t0001g0001 a0002c0002t0001g0015 a0002c0002t0001g0032 others(18): Show |
35 | HG00140.hp1 HG01069.hp2 HG01071.hp2 others(32): Show |
intron_variant | MODIFIER | c.2149-915C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871555 | |||||||
chr7:871598 | C | T | 7 | a0001c0001t0001g0137 a0001c0001t0001g0179 a0001c0001t0001g0180 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.2149-872C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871598 | |||||||
chr7:871626 | G | C | 6 | a0001c0001t0001g0041 a0001c0001t0001g0261 a0001c0001t0001g0263 others(3): Show |
6 | HG02647.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2149-844G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871626 | |||||||
chr7:871683 | CCACCCCG others(20): Show |
C | 1 | a0001c0001t0001g0137 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2149-786_2149-760d others(29): Show |
SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871683 | |||||||
chr7:871722 | A | G | 1 | a0001c0004t0002g0237 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.2149-748A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871722 | |||||||
chr7:871731 | A | G | 31 | a0001c0004t0002g0013 a0001c0004t0002g0014 a0001c0004t0002g0216 others(28): Show |
35 | HG00544.hp2 HG00621.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.2149-739A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871731 | |||||||
chr7:871742 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2149-728C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871742 | |||||||
chr7:871776 | A | G | 1 | a0008c0011t0006g0271 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2149-694A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871776 | |||||||
chr7:871870 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(262): Show |
317 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(314): Show |
intron_variant | MODIFIER | c.2149-600T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871870 | |||||||
chr7:871877 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2149-593A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 871877 | |||||||
chr7:872014 | G | C | 2 | a0001c0006t0012g0043 a0001c0006t0012g0044 |
2 | HG01243.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.2149-456G>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872014 | |||||||
chr7:872016 | C | T | 1 | a0002c0002t0001g0061 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2149-454C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872016 | |||||||
chr7:872020 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(261): Show |
316 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(313): Show |
intron_variant | MODIFIER | c.2149-450A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872020 | |||||||
chr7:872204 | T | C | 1 | a0001c0024t0001g0154 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2149-266T>C | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872204 | |||||||
chr7:872264 | A | G | 2 | a0001c0004t0002g0219 a0001c0004t0002g0220 |
2 | HG02132.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.2149-206A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872264 | |||||||
chr7:872319 | G | A | 7 | a0001c0006t0001g0019 a0001c0006t0001g0054 a0001c0006t0001g0055 others(4): Show |
8 | HG02257.hp2 HG02559.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.2149-151G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 17/18 | chr7 | 872319 | |||||||
chr7:872815 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0165 |
2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.2241+253G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 872815 | |||||||
chr7:872955 | C | T | 2 | a0003c0003t0001g0321 a0003c0003t0001g0322 |
2 | HG04115.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2242-260C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 872955 | |||||||
chr7:872960 | G | A | 2 | a0002c0005t0001g0023 a0002c0005t0001g0091 |
3 | HG00738.hp1 HG01884.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.2242-255G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 872960 | |||||||
chr7:873012 | G | A | 1 | a0002c0002t0009g0039 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2242-203G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873012 | |||||||
chr7:873015 | A | G | 7 | a0003c0003t0005g0272 a0003c0003t0005g0273 a0003c0012t0005g0274 others(4): Show |
7 | HG01106.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.2242-200A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873015 | |||||||
chr7:873034 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2242-181C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873034 | |||||||
chr7:873083 | T | A | 57 | a0003c0003t0001g0017 a0003c0003t0001g0037 a0003c0003t0001g0276 others(54): Show |
60 | HG00323.hp2 HG00408.hp2 HG00558.hp2 others(57): Show |
intron_variant | MODIFIER | c.2242-132T>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873083 | |||||||
chr7:873091 | A | G | 1 | a0001c0001t0001g0144 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2242-124A>G | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873091 | |||||||
chr7:873118 | C | T | 263 | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0007 others(260): Show |
315 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(312): Show |
intron_variant | MODIFIER | c.2242-97C>T | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873118 | |||||||
chr7:873137 | G | A | 1 | a0001c0006t0018g0260 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2242-78G>A | SUN1 | ENSG00000164828.18 | transcript | ENST00000401592.6 | protein_coding | 18/18 | chr7 | 873137 |