Item | Value |
---|---|
geneid | 342865 |
ensemblid | ENSG00000187135.8 |
hgncid | 33595 |
symbol | VSTM2B |
name | V-set and transmembrane domain containing 2B |
refseq_nuc | NM_001146339.2 |
refseq_prot | NP_001139811.1 |
ensembl_nuc | ENST00000335523.8 |
ensembl_prot | ENSP00000335038.6 |
mane_status | MANE Select |
chr | chr19 |
start | 29525994 |
end | 29564551 |
strand | + |
ver | v1.2 |
region | chr19:29525994-29564551 |
region5000 | chr19:29520994-29569551 |
regionname0 | VSTM2B_chr19_29525994_29564551 |
regionname5000 | VSTM2B_chr19_29520994_29569551 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 285 | 323 | 97 | 60 | 123 | 9 | 34 | 88 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
a0002 | 0/0 | 285 | 76 | 0 | 15 | 54 | 1 | 6 | 41 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
a0003 | 0/0 | 285 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
a0004 | 0/0 | 285 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
a0005 | 0/0 | 285 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
a0006 | 0/0 | 285 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
a0007 | 0/0 | 285 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | MEQRN others(280): Show |
chr19 | 29520994 | 29569551 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 855 | 278 | 77 | 55 | 105 | 7 | 34 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0001c0003 | 0/0 | 855 | 28 | 10 | 1 | 17 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0001c0004 | 0/0 | 855 | 15 | 10 | 2 | 1 | 2 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0001c0005 | 0/0 | 855 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0002c0002 | 0/0 | 855 | 76 | 0 | 15 | 54 | 1 | 6 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0003c0006 | 0/0 | 855 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0004c0007 | 0/0 | 855 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0005c0008 | 0/0 | 855 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0006c0009 | 0/0 | 855 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 | ||
a0007c0010 | 0/0 | 855 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | ATGGA others(850): Show |
chr19 | 29520994 | 29569551 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2065 | 262 | 71 | 53 | 101 | 6 | 31 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0002 | 0/0 | 2063 | 4 | 0 | 0 | 2 | 0 | 2 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2058): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0003 | 0/0 | 2065 | 3 | 3 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0004 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0005 | 0/0 | 2065 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0007 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0008 | 0/0 | 2065 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0009 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2058): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0010 | 0/0 | 2065 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0011 | 0/0 | 2065 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0001t0012 | 0/0 | 2065 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0003t0001 | 0/0 | 2065 | 25 | 9 | 1 | 15 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0003t0002 | 0/0 | 2063 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2058): Show |
chr19 | 29520994 | 29569551 |
a0001c0003t0003 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0003t0013 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0004t0001 | 0/0 | 2065 | 12 | 8 | 2 | 1 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0004t0002 | 0/0 | 2063 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2058): Show |
chr19 | 29520994 | 29569551 |
a0001c0004t0003 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0004t0004 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0001c0005t0001 | 0/0 | 2065 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0002c0002t0001 | 0/0 | 2065 | 62 | 0 | 14 | 41 | 1 | 6 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0002c0002t0002 | 0/0 | 2063 | 11 | 0 | 0 | 11 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2058): Show |
chr19 | 29520994 | 29569551 |
a0002c0002t0006 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0002c0002t0014 | 0/0 | 2065 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0002c0002t0015 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0003c0006t0001 | 0/0 | 2065 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0004c0007t0001 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0004c0007t0003 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0005c0008t0001 | 0/0 | 2065 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0006c0009t0001 | 0/0 | 2065 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
a0007c0010t0001 | 0/0 | 2065 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | GCCTC others(2060): Show |
chr19 | 29520994 | 29569551 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0004g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0007g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0009g0355 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0010g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0011g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0001t0012g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0003t0013g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0004t0004g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0001c0005t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0002 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0010 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0334 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0345 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0351 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0006g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0014g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0002c0002t0015g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0003c0006t0001g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0003c0006t0001g0344 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0004c0007t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0004c0007t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0005c0008t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0006c0009t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
a0007c0010t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | GBR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0181 | EUR | GBR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0326 | EUR | FIN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0333 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0047 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0313 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00438 | hp2 | a0002 | c0002 | t0001 | g0186 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00544 | hp2 | a0001 | c0003 | t0001 | g0051 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0352 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0336 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0351 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0302 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00673 | hp1 | a0002 | c0002 | t0001 | g0349 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | CHS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00733 | hp2 | a0005 | c0008 | t0001 | g0251 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00738 | hp1 | a0002 | c0002 | t0001 | g0319 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00738 | hp2 | a0002 | c0002 | t0001 | g0184 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG00741 | hp2 | a0001 | c0003 | t0001 | g0056 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0246 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0038 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01099 | hp1 | a0001 | c0001 | t0008 | g0222 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01109 | hp1 | a0001 | c0004 | t0001 | g0191 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01192 | hp1 | a0002 | c0002 | t0001 | g0337 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0338 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01243 | hp1 | a0002 | c0002 | t0014 | g0335 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0300 | AMR | PUR | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01256 | hp1 | a0001 | c0005 | t0001 | g0015 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0244 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01258 | hp2 | a0001 | c0005 | t0001 | g0015 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0218 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0249 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0301 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01361 | hp2 | a0001 | c0004 | t0001 | g0066 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0214 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0021 | EUR | IBS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | IBS | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0010 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02004 | hp2 | a0001 | c0001 | t0010 | g0109 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02015 | hp2 | a0001 | c0003 | t0001 | g0049 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02040 | hp1 | a0001 | c0004 | t0001 | g0074 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02056 | hp2 | a0002 | c0002 | t0002 | g0322 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02074 | hp1 | a0002 | c0002 | t0001 | g0248 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0303 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02132 | hp2 | a0002 | c0002 | t0002 | g0325 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0296 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02145 | hp2 | a0006 | c0009 | t0001 | g0283 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CDX | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CDX | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | CDX | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02165 | hp2 | a0001 | c0003 | t0001 | g0052 | EAS | CDX | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0262 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0332 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0348 | EAS | KHV | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02602 | hp2 | a0003 | c0006 | t0001 | g0344 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0258 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0210 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0252 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02717 | hp1 | a0004 | c0007 | t0003 | g0065 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02717 | hp2 | a0001 | c0003 | t0001 | g0060 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0299 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02738 | hp2 | a0002 | c0002 | t0001 | g0318 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0260 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02818 | hp2 | a0001 | c0001 | t0004 | g0155 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02895 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02895 | hp2 | a0001 | c0003 | t0001 | g0057 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02897 | hp1 | a0001 | c0003 | t0001 | g0013 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02922 | hp2 | a0001 | c0001 | t0005 | g0255 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02965 | hp1 | a0004 | c0007 | t0001 | g0064 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0193 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0290 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03017 | hp2 | a0002 | c0002 | t0001 | g0317 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0106 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0254 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0265 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0268 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0309 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0341 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03239 | hp1 | a0001 | c0001 | t0011 | g0297 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0189 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0354 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0306 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0070 | AFR | ESN | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03579 | hp1 | a0001 | c0004 | t0001 | g0030 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0310 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0327 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0304 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0227 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0314 | SAS | PJL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03942 | hp1 | a0003 | c0006 | t0001 | g0343 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0305 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | BEB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0240 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0295 | SAS | STU | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0192 | AFR | YRI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | CHB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | YRI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18906 | hp2 | a0001 | c0003 | t0001 | g0055 | AFR | YRI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18939 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18940 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0011 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18943 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18944 | hp1 | a0001 | c0001 | t0009 | g0355 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18944 | hp2 | a0001 | c0003 | t0002 | g0046 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18947 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18950 | hp2 | a0001 | c0003 | t0013 | g0045 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0350 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18953 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18953 | hp2 | a0002 | c0002 | t0001 | g0323 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18954 | hp2 | a0002 | c0002 | t0001 | g0320 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18957 | hp2 | a0001 | c0003 | t0001 | g0040 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18960 | hp1 | a0002 | c0002 | t0001 | g0329 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18960 | hp2 | a0001 | c0003 | t0001 | g0050 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0187 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18964 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18966 | hp2 | a0007 | c0010 | t0001 | g0149 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18969 | hp1 | a0001 | c0003 | t0001 | g0048 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18971 | hp1 | a0002 | c0002 | t0001 | g0353 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0331 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18977 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18979 | hp2 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18985 | hp2 | a0002 | c0002 | t0015 | g0039 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18986 | hp1 | a0002 | c0002 | t0001 | g0346 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18986 | hp2 | a0002 | c0002 | t0001 | g0321 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0307 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18992 | hp2 | a0002 | c0002 | t0001 | g0185 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18998 | hp1 | a0002 | c0002 | t0001 | g0347 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18998 | hp2 | a0002 | c0002 | t0001 | g0250 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0294 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19000 | hp1 | a0002 | c0002 | t0001 | g0316 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19001 | hp1 | a0002 | c0002 | t0002 | g0008 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19002 | hp2 | a0002 | c0002 | t0001 | g0293 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0330 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19006 | hp2 | a0002 | c0002 | t0001 | g0339 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19007 | hp1 | a0002 | c0002 | t0002 | g0328 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19012 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0206 | AFR | LWK | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0085 | AFR | LWK | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19043 | hp1 | a0001 | c0003 | t0003 | g0058 | AFR | LWK | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | LWK | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19054 | hp1 | a0002 | c0002 | t0001 | g0264 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19054 | hp2 | a0001 | c0003 | t0001 | g0042 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0334 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19058 | hp2 | a0002 | c0002 | t0006 | g0311 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19065 | hp1 | a0001 | c0003 | t0001 | g0188 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0298 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0345 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0053 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19077 | hp2 | a0002 | c0002 | t0002 | g0037 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19086 | hp2 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19088 | hp1 | a0001 | c0003 | t0001 | g0044 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | YRI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20129 | hp1 | a0001 | c0003 | t0001 | g0054 | AFR | ASW | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0190 | AFR | ASW | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20752 | hp1 | a0001 | c0004 | t0002 | g0199 | EUR | TSI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0113 | EUR | TSI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20805 | hp1 | a0001 | c0001 | t0012 | g0232 | EUR | TSI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20805 | hp2 | a0001 | c0004 | t0001 | g0200 | EUR | TSI | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | GIH | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02109 | hp1 | a0001 | c0004 | t0004 | g0063 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0253 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0261 | AFR | ACB | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0012 | AFR | MSL | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG06807 | hp1 | a0001 | c0004 | t0001 | g0202 | AFR | USA | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | USA | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0292 | EAS | JPT | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20300 | hp1 | a0001 | c0004 | t0003 | g0194 | AFR | USA | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | USA | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA21309 | hp1 | a0001 | c0001 | t0005 | g0256 | AFR | LWK | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
NA21309 | hp2 | a0001 | c0004 | t0001 | g0201 | AFR | LWK | VSTM2B_chr19_29520994_29569551 | VSTM2B | chr19 | 29520994 | 29569551 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:29527379 | C | G | 1 | a0007 | 1 | NA18966.hp2 | missense_variant | MODERATE | c.251C>G | p.Pro84Arg | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/5 | 841/2065 | 251/858 | 84/285 | chr19 | 29527379 | |||
chr19:29528442 | A | G | 1 | a0006 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.277A>G | p.Lys93Glu | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/5 | 867/2065 | 277/858 | 93/285 | chr19 | 29528442 | |||
chr19:29529853 | G | A | 1 | a0004 | 2 | HG02717.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.332G>A | p.Arg111Gln | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/5 | 922/2065 | 332/858 | 111/285 | chr19 | 29529853 | |||
chr19:29530116 | G | C | 2 | a0002 a0003 |
78 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
missense_variant | MODERATE | c.595G>C | p.Asp199His | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/5 | 1185/2065 | 595/858 | 199/285 | chr19 | 29530116 | |||
chr19:29530176 | G | A | 1 | a0005 | 1 | HG00733.hp2 | missense_variant | MODERATE | c.655G>A | p.Ala219Thr | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/5 | 1245/2065 | 655/858 | 219/285 | chr19 | 29530176 | |||
chr19:29530224 | G | A | 1 | a0003 | 2 | HG02602.hp2 HG03942.hp1 |
missense_variant | MODERATE | c.703G>A | p.Ala235Thr | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/5 | 1293/2065 | 703/858 | 235/285 | chr19 | 29530224 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:29527383 | C | A | 1 | a0001c0005 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.255C>A | p.Gly85Gly | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/5 | 845/2065 | 255/858 | 85/285 | chr19 | 29527383 | |||
chr19:29529845 | C | T | 2 | a0001c0004 a0004c0007 |
17 | HG01109.hp1 HG01361.hp2 HG02040.hp1 others(14): Show |
synonymous_variant | LOW | c.324C>T | p.Ile108Ile | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/5 | 914/2065 | 324/858 | 108/285 | chr19 | 29529845 | |||
chr19:29530187 | G | C | 1 | a0001c0003 | 28 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(25): Show |
synonymous_variant | LOW | c.666G>C | p.Ser222Ser | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/5 | 1256/2065 | 666/858 | 222/285 | chr19 | 29530187 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:29526110 | C | G | 1 | a0002c0002t0015 | 1 | NA18985.hp2 | 5_prime_UTR_variant | MODIFIER | c.-474C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 474 | chr19 | 29526110 | ||||||
chr19:29526141 | C | G | 1 | a0002c0002t0014 | 1 | HG01243.hp1 | 5_prime_UTR_variant | MODIFIER | c.-443C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 443 | chr19 | 29526141 | ||||||
chr19:29526160 | G | A | 1 | a0002c0002t0006 | 1 | NA19058.hp2 | 5_prime_UTR_variant | MODIFIER | c.-424G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 424 | chr19 | 29526160 | ||||||
chr19:29526167 | A | T | 1 | a0001c0003t0013 | 1 | NA18950.hp2 | 5_prime_UTR_variant | MODIFIER | c.-417A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 417 | chr19 | 29526167 | ||||||
chr19:29526226 | G | A | 1 | a0002c0002t0015 | 1 | NA18985.hp2 | 5_prime_UTR_variant | MODIFIER | c.-358G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 358 | chr19 | 29526226 | ||||||
chr19:29526454 | G | A | 1 | a0001c0001t0007 | 1 | NA18943.hp1 | 5_prime_UTR_variant | MODIFIER | c.-130G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 130 | chr19 | 29526454 | ||||||
chr19:29526462 | G | A | 1 | a0001c0001t0008 | 1 | HG01099.hp1 | 5_prime_UTR_variant | MODIFIER | c.-122G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 122 | chr19 | 29526462 | ||||||
chr19:29526526 | A | T | 1 | a0001c0001t0012 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 58 | chr19 | 29526526 | ||||||
chr19:29526528 | G | T | 1 | a0001c0001t0011 | 1 | HG03239.hp1 | 5_prime_UTR_variant | MODIFIER | c.-56G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/5 | 56 | chr19 | 29526528 | ||||||
chr19:29563966 | C | T | 4 | a0001c0001t0003 a0001c0003t0003 a0001c0004t0003 others(1): Show |
6 | HG02717.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*32C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 5/5 | 32 | chr19 | 29563966 | ||||||
chr19:29563990 | C | T | 1 | a0001c0001t0010 | 1 | HG02004.hp2 | 3_prime_UTR_variant | MODIFIER | c.*56C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 5/5 | 56 | chr19 | 29563990 | ||||||
chr19:29564018 | CAG | C | 5 | a0001c0001t0002 a0001c0001t0009 a0001c0003t0002 others(2): Show |
18 | HG00544.hp1 HG02056.hp2 HG02132.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*90_*91delGA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 5/5 | 90 | INFO_REALIGN_3_PRIME | chr19 | 29564018 | |||||
chr19:29564120 | G | C | 1 | a0001c0001t0009 | 1 | NA18944.hp1 | 3_prime_UTR_variant | MODIFIER | c.*186G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 5/5 | 186 | chr19 | 29564120 | ||||||
chr19:29564467 | G | A | 2 | a0001c0001t0004 a0001c0004t0004 |
2 | HG02109.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*533G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 5/5 | 533 | chr19 | 29564467 | ||||||
chr19:29564469 | T | C | 1 | a0001c0001t0005 | 2 | HG02922.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*535T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 5/5 | 535 | chr19 | 29564469 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:29526758 | G | C | 1 | a0002c0002t0015g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.82+93G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29526758 | |||||||
chr19:29526759 | C | G | 1 | a0002c0002t0015g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.82+94C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29526759 | |||||||
chr19:29526763 | G | A | 24 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(21): Show |
27 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.82+98G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29526763 | |||||||
chr19:29526852 | C | G | 118 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0253 others(115): Show |
131 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.82+187C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29526852 | |||||||
chr19:29526872 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.82+207G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29526872 | |||||||
chr19:29527084 | C | G | 1 | a0002c0002t0015g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.83-127C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29527084 | |||||||
chr19:29527085 | G | C | 1 | a0002c0002t0015g0039 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.83-126G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29527085 | |||||||
chr19:29527142 | C | T | 3 | a0001c0001t0001g0007 a0001c0001t0001g0245 a0001c0001t0001g0246 |
5 | HG00735.hp2 HG01069.hp1 HG01257.hp1 others(2): Show |
intron_variant | MODIFIER | c.83-69C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29527142 | |||||||
chr19:29527145 | G | T | 41 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(38): Show |
47 | HG00408.hp2 HG00597.hp2 HG00735.hp1 others(44): Show |
intron_variant | MODIFIER | c.83-66G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29527145 | |||||||
chr19:29527149 | T | C | 1 | a0001c0001t0001g0062 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.83-62T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 1/4 | chr19 | 29527149 | |||||||
chr19:29527403 | G | A | 15 | a0001c0003t0001g0011 a0001c0003t0001g0040 a0001c0003t0001g0041 others(12): Show |
16 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(13): Show |
splice_region_variant&intron_variant | LOW | c.267+8G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527403 | |||||||
chr19:29527406 | G | C | 1 | a0001c0001t0001g0247 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.267+11G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527406 | |||||||
chr19:29527419 | C | A | 3 | a0001c0004t0004g0063 a0004c0007t0001g0064 a0004c0007t0003g0065 |
3 | HG02109.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.267+24C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527419 | |||||||
chr19:29527462 | A | G | 156 | a0001c0001t0001g0036 a0001c0001t0001g0198 a0001c0001t0001g0203 others(153): Show |
172 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(169): Show |
intron_variant | MODIFIER | c.267+67A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527462 | |||||||
chr19:29527516 | C | G | 1 | a0001c0001t0001g0197 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.267+121C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527516 | |||||||
chr19:29527543 | T | C | 1 | a0001c0004t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.267+148T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527543 | |||||||
chr19:29527573 | C | T | 3 | a0001c0004t0004g0063 a0004c0007t0001g0064 a0004c0007t0003g0065 |
3 | HG02109.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.267+178C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527573 | |||||||
chr19:29527733 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0009g0355 |
2 | NA18944.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.267+338C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527733 | |||||||
chr19:29527826 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+431C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527826 | |||||||
chr19:29527851 | C | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+456C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527851 | |||||||
chr19:29527860 | G | A | 1 | a0001c0001t0001g0209 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.267+465G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527860 | |||||||
chr19:29527861 | C | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.267+466C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29527861 | |||||||
chr19:29528008 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.268-425A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29528008 | |||||||
chr19:29528294 | T | A | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.268-139T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29528294 | |||||||
chr19:29528341 | G | A | 1 | a0002c0002t0001g0248 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.268-92G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29528341 | |||||||
chr19:29528423 | T | C | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.268-10T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29528423 | |||||||
chr19:29528426 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02040.hp2 | splice_region_variant&intron_variant | LOW | c.268-7A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 2/4 | chr19 | 29528426 | |||||||
chr19:29528495 | A | T | 3 | a0001c0004t0001g0030 a0001c0004t0001g0193 a0001c0004t0003g0194 |
4 | HG02965.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+33A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528495 | |||||||
chr19:29528532 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.297+70C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528532 | |||||||
chr19:29528557 | T | G | 1 | a0001c0001t0001g0069 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.297+95T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528557 | |||||||
chr19:29528598 | C | T | 38 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(35): Show |
42 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.297+136C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528598 | |||||||
chr19:29528602 | G | A | 3 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG01891.hp1 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.297+140G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528602 | |||||||
chr19:29528676 | C | T | 8 | a0001c0004t0001g0030 a0001c0004t0001g0066 a0001c0004t0001g0189 others(5): Show |
9 | HG01109.hp1 HG01361.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.297+214C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528676 | |||||||
chr19:29528770 | C | T | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+308C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528770 | |||||||
chr19:29528794 | A | T | 1 | a0001c0001t0001g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.297+332A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528794 | |||||||
chr19:29528926 | G | C | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+464G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528926 | |||||||
chr19:29528932 | G | T | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.297+470G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29528932 | |||||||
chr19:29529008 | A | G | 9 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0054 others(6): Show |
11 | HG00741.hp2 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.297+546A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529008 | |||||||
chr19:29529035 | T | A | 3 | a0001c0004t0001g0030 a0001c0004t0001g0193 a0001c0004t0003g0194 |
4 | HG02965.hp2 HG03225.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.297+573T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529035 | |||||||
chr19:29529048 | G | C | 1 | a0001c0001t0001g0210 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.297+586G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529048 | |||||||
chr19:29529156 | C | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.298-663C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529156 | |||||||
chr19:29529180 | G | C | 1 | a0002c0002t0001g0250 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.298-639G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529180 | |||||||
chr19:29529280 | C | G | 167 | a0001c0001t0001g0036 a0001c0001t0001g0203 a0001c0001t0001g0204 others(164): Show |
184 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(181): Show |
intron_variant | MODIFIER | c.298-539C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529280 | |||||||
chr19:29529374 | GC | G | 8 | a0001c0004t0001g0030 a0001c0004t0001g0066 a0001c0004t0001g0189 others(5): Show |
9 | HG01109.hp1 HG01361.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.298-443delC | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr19 | 29529374 | ||||||
chr19:29529384 | G | C | 1 | a0001c0001t0001g0073 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.298-435G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529384 | |||||||
chr19:29529385 | C | G | 1 | a0001c0001t0001g0073 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.298-434C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529385 | |||||||
chr19:29529771 | T | C | 170 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0001c0001t0001g0198 others(167): Show |
187 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.298-48T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 3/4 | chr19 | 29529771 | |||||||
chr19:29530312 | G | A | 1 | a0002c0002t0001g0252 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.769+22G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530312 | |||||||
chr19:29530401 | C | T | 9 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0054 others(6): Show |
11 | HG00741.hp2 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+111C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530401 | |||||||
chr19:29530435 | G | GC | 14 | a0001c0001t0001g0075 a0001c0004t0001g0030 a0001c0004t0001g0066 others(11): Show |
15 | HG01109.hp1 HG01361.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.769+153dupC | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29530435 | ||||||
chr19:29530438 | C | CT | 31 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(28): Show |
34 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.769+148_769+149ins others(1): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530438 | |||||||
chr19:29530443 | C | CT | 105 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0267 others(102): Show |
118 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.769+153_769+154ins others(1): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530443 | |||||||
chr19:29530443 | C | T | 32 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(29): Show |
35 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(32): Show |
intron_variant | MODIFIER | c.769+153C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530443 | |||||||
chr19:29530539 | G | A | 20 | a0001c0001t0001g0267 a0001c0001t0001g0269 a0001c0001t0001g0270 others(17): Show |
20 | HG00558.hp1 HG00597.hp1 HG02055.hp2 others(17): Show |
intron_variant | MODIFIER | c.769+249G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530539 | |||||||
chr19:29530591 | G | A | 1 | a0001c0001t0001g0253 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.769+301G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530591 | |||||||
chr19:29530598 | G | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(22): Show |
28 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.769+308G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530598 | |||||||
chr19:29530618 | A | T | 4 | a0001c0001t0001g0029 a0001c0001t0001g0181 a0001c0001t0001g0182 others(1): Show |
5 | HG00140.hp2 HG02486.hp1 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+328A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530618 | |||||||
chr19:29530653 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.769+363C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530653 | |||||||
chr19:29530701 | G | T | 3 | a0001c0004t0004g0063 a0004c0007t0001g0064 a0004c0007t0003g0065 |
3 | HG02109.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+411G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530701 | |||||||
chr19:29530846 | G | C | 25 | a0001c0003t0001g0011 a0001c0003t0001g0012 a0001c0003t0001g0013 others(22): Show |
28 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.769+556G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530846 | |||||||
chr19:29530878 | C | T | 1 | a0001c0001t0001g0266 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.769+588C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530878 | |||||||
chr19:29530913 | C | T | 9 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0054 others(6): Show |
11 | HG00741.hp2 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+623C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29530913 | |||||||
chr19:29531000 | A | G | 31 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(28): Show |
34 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.769+710A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531000 | |||||||
chr19:29531113 | T | C | 17 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0076 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.769+823T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531113 | |||||||
chr19:29531116 | G | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG00673.hp2 NA18939.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+826G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531116 | |||||||
chr19:29531520 | C | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0025 others(72): Show |
87 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.769+1230C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531520 | |||||||
chr19:29531643 | G | A | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+1353G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531643 | |||||||
chr19:29531757 | A | T | 9 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0054 others(6): Show |
11 | HG00741.hp2 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+1467A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531757 | |||||||
chr19:29531873 | G | A | 8 | a0001c0001t0001g0247 a0001c0001t0001g0287 a0001c0001t0001g0288 others(5): Show |
8 | HG00733.hp2 HG02083.hp2 HG02683.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+1583G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531873 | |||||||
chr19:29531976 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.769+1686T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29531976 | |||||||
chr19:29532090 | C | T | 5 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0004t0001g0202 others(2): Show |
5 | HG06807.hp1 NA18971.hp1 NA20752.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+1800C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532090 | |||||||
chr19:29532154 | G | A | 26 | a0001c0001t0001g0267 a0001c0003t0001g0011 a0001c0003t0001g0012 others(23): Show |
29 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.769+1864G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532154 | |||||||
chr19:29532253 | C | T | 1 | a0001c0001t0001g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.769+1963C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532253 | |||||||
chr19:29532296 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0158 a0001c0001t0001g0159 |
4 | NA18948.hp2 NA18971.hp2 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+2006G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532296 | |||||||
chr19:29532302 | A | T | 4 | a0002c0002t0001g0349 a0002c0002t0001g0350 a0002c0002t0001g0351 others(1): Show |
4 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+2012A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532302 | |||||||
chr19:29532316 | G | C | 1 | a0001c0001t0001g0094 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.769+2026G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532316 | |||||||
chr19:29532323 | G | A | 1 | a0001c0001t0003g0268 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.769+2033G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532323 | |||||||
chr19:29532386 | A | G | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.769+2096A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532386 | |||||||
chr19:29532455 | G | A | 1 | a0001c0001t0001g0254 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.769+2165G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532455 | |||||||
chr19:29532580 | C | T | 1 | a0001c0003t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.769+2290C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532580 | |||||||
chr19:29532669 | T | C | 9 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0054 others(6): Show |
11 | HG00741.hp2 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+2379T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532669 | |||||||
chr19:29532860 | C | T | 1 | a0001c0003t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.769+2570C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532860 | |||||||
chr19:29532909 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.769+2619C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532909 | |||||||
chr19:29532925 | G | A | 5 | a0001c0001t0001g0075 a0001c0004t0001g0030 a0001c0004t0001g0074 others(2): Show |
6 | HG02040.hp1 HG02965.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+2635G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29532925 | |||||||
chr19:29533046 | G | A | 1 | a0001c0004t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.769+2756G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533046 | |||||||
chr19:29533153 | C | T | 4 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0004t0001g0202 others(1): Show |
4 | HG06807.hp1 NA20752.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+2863C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533153 | |||||||
chr19:29533356 | T | A | 2 | a0001c0003t0001g0054 a0001c0003t0001g0055 |
2 | NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.769+3066T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533356 | |||||||
chr19:29533469 | T | C | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.769+3179T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533469 | |||||||
chr19:29533490 | C | A | 40 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0003t0001g0011 others(37): Show |
44 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.769+3200C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533490 | |||||||
chr19:29533528 | C | T | 1 | a0001c0001t0001g0291 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.769+3238C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533528 | |||||||
chr19:29533610 | TG | T | 9 | a0001c0003t0001g0012 a0001c0003t0001g0013 a0001c0003t0001g0054 others(6): Show |
11 | HG00741.hp2 HG02257.hp2 HG02717.hp2 others(8): Show |
intron_variant | MODIFIER | c.769+3321delG | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533610 | |||||||
chr19:29533638 | T | C | 1 | a0002c0002t0001g0293 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.769+3348T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533638 | |||||||
chr19:29533676 | C | G | 4 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0197 others(1): Show |
4 | HG02630.hp2 HG02647.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+3386C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533676 | |||||||
chr19:29533695 | A | G | 1 | a0002c0002t0002g0348 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.769+3405A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533695 | |||||||
chr19:29533823 | A | C | 170 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0096 others(167): Show |
187 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(184): Show |
intron_variant | MODIFIER | c.769+3533A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533823 | |||||||
chr19:29533843 | G | T | 1 | a0001c0001t0001g0073 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.769+3553G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533843 | |||||||
chr19:29533855 | C | A | 1 | a0001c0003t0001g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.769+3565C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533855 | |||||||
chr19:29533866 | G | A | 166 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0096 others(163): Show |
183 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(180): Show |
intron_variant | MODIFIER | c.769+3576G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533866 | |||||||
chr19:29533892 | G | C | 1 | a0005c0008t0001g0251 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.769+3602G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533892 | |||||||
chr19:29533908 | C | T | 32 | a0001c0001t0001g0029 a0001c0001t0001g0095 a0001c0001t0001g0096 others(29): Show |
36 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.769+3618C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533908 | |||||||
chr19:29533914 | TG | T | 3 | a0001c0004t0004g0063 a0004c0007t0001g0064 a0004c0007t0003g0065 |
3 | HG02109.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+3627delG | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29533914 | ||||||
chr19:29533949 | C | T | 3 | a0001c0004t0004g0063 a0004c0007t0001g0064 a0004c0007t0003g0065 |
3 | HG02109.hp1 HG02717.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.769+3659C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29533949 | |||||||
chr19:29534245 | A | C | 2 | a0001c0001t0001g0254 a0001c0001t0001g0265 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.769+3955A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534245 | |||||||
chr19:29534303 | T | G | 1 | a0002c0002t0001g0294 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.769+4013T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534303 | |||||||
chr19:29534463 | A | C | 146 | a0001c0001t0001g0024 a0001c0001t0001g0036 a0001c0001t0001g0075 others(143): Show |
163 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(160): Show |
intron_variant | MODIFIER | c.769+4173A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534463 | |||||||
chr19:29534716 | C | CA | 45 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0032 others(42): Show |
51 | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(48): Show |
intron_variant | MODIFIER | c.769+4439dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29534716 | ||||||
chr19:29534716 | CA | C | 52 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0076 others(49): Show |
54 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.769+4439delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29534716 | ||||||
chr19:29534726 | A | AAAG | 125 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0001c0001t0001g0247 others(122): Show |
139 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.769+4438_769+4439i others(5): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29534726 | ||||||
chr19:29534753 | A | G | 17 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0076 others(14): Show |
17 | HG01884.hp1 HG02055.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.769+4463A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534753 | |||||||
chr19:29534799 | C | CG | 4 | a0001c0001t0001g0073 a0001c0001t0001g0097 a0001c0003t0001g0041 others(1): Show |
4 | HG03098.hp1 NA18992.hp2 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+4511dupG | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29534799 | ||||||
chr19:29534826 | C | G | 107 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0267 others(104): Show |
120 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.769+4536C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534826 | |||||||
chr19:29534882 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.769+4592A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534882 | |||||||
chr19:29534902 | C | T | 127 | a0001c0001t0001g0036 a0001c0001t0001g0075 a0001c0001t0001g0247 others(124): Show |
141 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(138): Show |
intron_variant | MODIFIER | c.769+4612C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29534902 | |||||||
chr19:29535027 | T | C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0099 a0001c0001t0001g0100 |
3 | NA18967.hp1 NA19010.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.769+4737T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535027 | |||||||
chr19:29535073 | C | T | 2 | a0001c0004t0001g0191 a0001c0004t0001g0192 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+4783C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535073 | |||||||
chr19:29535110 | C | G | 135 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0253 others(132): Show |
151 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.769+4820C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535110 | |||||||
chr19:29535131 | G | A | 1 | a0001c0001t0001g0211 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.769+4841G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535131 | |||||||
chr19:29535388 | G | C | 164 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0096 others(161): Show |
181 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.769+5098G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535388 | |||||||
chr19:29535476 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.769+5186G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535476 | |||||||
chr19:29535479 | T | G | 4 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0004t0001g0202 others(1): Show |
4 | HG06807.hp1 NA20752.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5189T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535479 | |||||||
chr19:29535576 | T | C | 164 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0096 others(161): Show |
181 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.769+5286T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535576 | |||||||
chr19:29535592 | G | C | 1 | a0001c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.769+5302G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535592 | |||||||
chr19:29535636 | C | G | 4 | a0002c0002t0001g0293 a0002c0002t0001g0345 a0002c0002t0001g0346 others(1): Show |
4 | NA18986.hp1 NA18998.hp1 NA19002.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5346C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535636 | |||||||
chr19:29535652 | C | T | 4 | a0001c0001t0001g0152 a0001c0001t0001g0243 a0003c0006t0001g0343 others(1): Show |
4 | HG01081.hp2 HG02027.hp1 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5362C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535652 | |||||||
chr19:29535666 | G | A | 3 | a0001c0003t0001g0054 a0001c0003t0001g0055 a0001c0003t0001g0056 |
3 | HG00741.hp2 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.769+5376G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535666 | |||||||
chr19:29535744 | G | C | 1 | a0001c0004t0004g0063 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.769+5454G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535744 | |||||||
chr19:29535835 | C | T | 107 | a0001c0001t0001g0036 a0001c0001t0001g0247 a0001c0001t0001g0267 others(104): Show |
120 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.769+5545C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535835 | |||||||
chr19:29535847 | A | G | 1 | a0001c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.769+5557A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535847 | |||||||
chr19:29535854 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.769+5564C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535854 | |||||||
chr19:29535863 | G | A | 1 | a0001c0001t0001g0271 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.769+5573G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535863 | |||||||
chr19:29535864 | A | G | 5 | a0001c0003t0001g0013 a0001c0003t0001g0054 a0001c0003t0001g0055 others(2): Show |
6 | HG00741.hp2 HG02717.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.769+5574A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535864 | |||||||
chr19:29535984 | G | A | 1 | a0002c0002t0001g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.769+5694G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535984 | |||||||
chr19:29535985 | C | T | 4 | a0001c0004t0001g0200 a0001c0004t0001g0201 a0001c0004t0001g0202 others(1): Show |
4 | HG06807.hp1 NA20752.hp1 NA20805.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+5695C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29535985 | |||||||
chr19:29536110 | G | T | 1 | a0001c0001t0001g0151 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.769+5820G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536110 | |||||||
chr19:29536174 | C | T | 6 | a0001c0004t0001g0030 a0001c0004t0001g0066 a0001c0004t0001g0189 others(3): Show |
7 | HG01361.hp2 HG02965.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+5884C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536174 | |||||||
chr19:29536178 | A | G | 146 | a0001c0001t0001g0036 a0001c0001t0001g0203 a0001c0001t0001g0204 others(143): Show |
162 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
intron_variant | MODIFIER | c.769+5888A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536178 | |||||||
chr19:29536201 | G | A | 2 | a0001c0004t0001g0191 a0001c0004t0001g0192 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.769+5911G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536201 | |||||||
chr19:29536216 | A | G | 164 | a0001c0001t0001g0036 a0001c0001t0001g0095 a0001c0001t0001g0096 others(161): Show |
181 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(178): Show |
intron_variant | MODIFIER | c.769+5926A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536216 | |||||||
chr19:29536227 | G | A | 1 | a0001c0001t0001g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.769+5937G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536227 | |||||||
chr19:29536252 | C | T | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.769+5962C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536252 | |||||||
chr19:29536393 | C | T | 1 | a0001c0001t0001g0089 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.769+6103C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536393 | |||||||
chr19:29536569 | C | T | 1 | a0001c0001t0001g0150 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.769+6279C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536569 | |||||||
chr19:29536665 | G | T | 6 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01074.hp1 HG01256.hp2 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+6375G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29536665 | |||||||
chr19:29537030 | T | C | 6 | a0001c0001t0001g0024 a0001c0003t0001g0012 a0001c0003t0001g0057 others(3): Show |
9 | HG02257.hp2 HG02895.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+6740T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537030 | |||||||
chr19:29537033 | C | T | 1 | a0001c0001t0001g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.769+6743C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537033 | |||||||
chr19:29537058 | G | A | 1 | a0001c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.769+6768G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537058 | |||||||
chr19:29537065 | T | C | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.769+6775T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537065 | |||||||
chr19:29537073 | T | TTGTA | 4 | a0001c0003t0001g0012 a0001c0003t0001g0057 a0001c0003t0001g0059 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+6785_769+6788d others(6): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29537073 | ||||||
chr19:29537116 | G | A | 2 | a0001c0001t0001g0254 a0001c0001t0001g0265 |
2 | HG03139.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.769+6826G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537116 | |||||||
chr19:29537183 | T | C | 1 | a0001c0001t0001g0354 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.769+6893T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537183 | |||||||
chr19:29537278 | T | G | 2 | a0001c0004t0001g0193 a0001c0004t0003g0194 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.769+6988T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537278 | |||||||
chr19:29537397 | G | A | 2 | a0001c0001t0001g0180 a0001c0003t0001g0060 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.769+7107G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537397 | |||||||
chr19:29537445 | T | A | 2 | a0001c0001t0001g0210 a0001c0004t0001g0074 |
2 | HG02040.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.769+7155T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537445 | |||||||
chr19:29537532 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.769+7242T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537532 | |||||||
chr19:29537673 | G | A | 1 | a0001c0001t0001g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.769+7383G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537673 | |||||||
chr19:29537703 | A | ACACCCAC others(11): Show |
5 | a0001c0001t0001g0180 a0001c0001t0001g0214 a0001c0001t0001g0244 others(2): Show |
5 | HG01257.hp2 HG01496.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+7456_769+7473d others(20): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29537703 | ||||||
chr19:29537703 | A | ACACCCAC others(29): Show |
14 | a0001c0001t0001g0016 a0001c0001t0001g0024 a0001c0001t0001g0068 others(11): Show |
18 | HG00639.hp2 HG01243.hp2 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.769+7438_769+7473d others(38): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29537703 | ||||||
chr19:29537703 | A | ACACCCAC others(47): Show |
21 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0098 others(18): Show |
22 | HG00423.hp2 HG00544.hp2 HG00609.hp2 others(19): Show |
intron_variant | MODIFIER | c.769+7420_769+7473d others(56): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29537703 | ||||||
chr19:29537703 | ACACCCAC others(11): Show |
A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0196 others(2): Show |
5 | HG01361.hp2 HG03130.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+7456_769+7473d others(20): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29537703 | ||||||
chr19:29537713 | A | T | 1 | a0001c0001t0001g0178 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.769+7423A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537713 | |||||||
chr19:29537716 | C | G | 1 | a0001c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.769+7426C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537716 | |||||||
chr19:29537739 | G | A | 2 | a0001c0004t0001g0200 a0001c0004t0002g0199 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.769+7449G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537739 | |||||||
chr19:29537751 | T | C | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.769+7461T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537751 | |||||||
chr19:29537751 | T | TCTCCCGC others(29): Show |
12 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(9): Show |
14 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(11): Show |
intron_variant | MODIFIER | c.769+7473_769+7474i others(38): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29537751 | ||||||
chr19:29537920 | C | T | 2 | a0001c0001t0001g0180 a0001c0003t0001g0060 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.769+7630C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29537920 | |||||||
chr19:29538033 | G | T | 1 | a0001c0003t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.769+7743G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538033 | |||||||
chr19:29538034 | T | C | 7 | a0001c0001t0001g0024 a0001c0001t0001g0105 a0001c0001t0001g0107 others(4): Show |
8 | HG02896.hp1 HG02897.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+7744T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538034 | |||||||
chr19:29538247 | C | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+7957C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538247 | |||||||
chr19:29538251 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+7961A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538251 | |||||||
chr19:29538264 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.769+7974T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538264 | |||||||
chr19:29538286 | C | T | 3 | a0001c0001t0004g0155 a0001c0004t0001g0193 a0001c0004t0003g0194 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.769+7996C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538286 | |||||||
chr19:29538320 | G | A | 26 | a0001c0001t0001g0016 a0001c0001t0001g0061 a0001c0001t0001g0095 others(23): Show |
28 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(25): Show |
intron_variant | MODIFIER | c.769+8030G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538320 | |||||||
chr19:29538331 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.769+8041C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538331 | |||||||
chr19:29538333 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+8043G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538333 | |||||||
chr19:29538442 | G | A | 2 | a0001c0001t0001g0181 a0001c0001t0001g0274 |
2 | HG00140.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.769+8152G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538442 | |||||||
chr19:29538468 | G | A | 1 | a0002c0002t0001g0035 | 2 | NA18952.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.769+8178G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538468 | |||||||
chr19:29538481 | C | T | 1 | a0007c0010t0001g0149 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.769+8191C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538481 | |||||||
chr19:29538502 | C | T | 20 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0098 others(17): Show |
21 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(18): Show |
intron_variant | MODIFIER | c.769+8212C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538502 | |||||||
chr19:29538529 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+8239C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538529 | |||||||
chr19:29538546 | C | A | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.769+8256C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538546 | |||||||
chr19:29538575 | C | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+8285C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538575 | |||||||
chr19:29538605 | G | T | 8 | a0001c0001t0004g0155 a0001c0003t0001g0012 a0001c0003t0001g0057 others(5): Show |
9 | HG02257.hp2 HG02818.hp2 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.769+8315G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538605 | |||||||
chr19:29538637 | A | G | 210 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(207): Show |
237 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.769+8347A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538637 | |||||||
chr19:29538643 | G | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+8353G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538643 | |||||||
chr19:29538646 | A | G | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.769+8356A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538646 | |||||||
chr19:29538715 | A | G | 1 | a0001c0001t0001g0180 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.769+8425A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538715 | |||||||
chr19:29538878 | T | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+8588T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538878 | |||||||
chr19:29538967 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.769+8677T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29538967 | |||||||
chr19:29539012 | C | T | 1 | a0001c0003t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.769+8722C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539012 | |||||||
chr19:29539013 | G | A | 5 | a0001c0001t0001g0003 a0001c0001t0001g0110 a0001c0001t0001g0215 others(2): Show |
7 | HG01255.hp1 HG01361.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+8723G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539013 | |||||||
chr19:29539024 | GT | G | 3 | a0001c0001t0004g0155 a0001c0004t0001g0193 a0001c0004t0003g0194 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.769+8739delT | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29539024 | ||||||
chr19:29539131 | C | T | 17 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0273 others(14): Show |
18 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(15): Show |
intron_variant | MODIFIER | c.769+8841C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539131 | |||||||
chr19:29539207 | C | T | 1 | a0001c0003t0001g0060 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.769+8917C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539207 | |||||||
chr19:29539210 | C | T | 2 | a0001c0001t0001g0180 a0001c0003t0001g0060 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.769+8920C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539210 | |||||||
chr19:29539296 | G | T | 7 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+9006G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539296 | |||||||
chr19:29539297 | C | T | 7 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+9007C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539297 | |||||||
chr19:29539308 | G | A | 2 | a0001c0001t0001g0103 a0001c0003t0001g0060 |
2 | HG02717.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.769+9018G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539308 | |||||||
chr19:29539310 | G | A | 1 | a0001c0001t0001g0287 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.769+9020G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539310 | |||||||
chr19:29539328 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.769+9038G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539328 | |||||||
chr19:29539343 | G | T | 1 | a0002c0002t0001g0347 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.769+9053G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539343 | |||||||
chr19:29539516 | C | T | 7 | a0001c0001t0001g0034 a0001c0001t0001g0103 a0001c0001t0001g0236 others(4): Show |
8 | NA18948.hp1 NA18966.hp1 NA18977.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+9226C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539516 | |||||||
chr19:29539527 | A | G | 1 | a0001c0001t0001g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.769+9237A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539527 | |||||||
chr19:29539571 | C | T | 5 | a0002c0002t0001g0185 a0002c0002t0001g0293 a0002c0002t0001g0345 others(2): Show |
5 | NA18986.hp1 NA18992.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+9281C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539571 | |||||||
chr19:29539625 | G | A | 1 | a0001c0003t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.769+9335G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539625 | |||||||
chr19:29539644 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.769+9354C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539644 | |||||||
chr19:29539645 | G | A | 53 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(50): Show |
63 | HG00140.hp1 HG00438.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.769+9355G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539645 | |||||||
chr19:29539671 | G | A | 210 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0016 others(207): Show |
237 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(234): Show |
intron_variant | MODIFIER | c.769+9381G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539671 | |||||||
chr19:29539694 | C | A | 7 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+9404C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539694 | |||||||
chr19:29539694 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+9404C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539694 | |||||||
chr19:29539743 | G | A | 21 | a0001c0001t0001g0061 a0001c0001t0001g0086 a0001c0001t0001g0087 others(18): Show |
22 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.769+9453G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539743 | |||||||
chr19:29539807 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0196 others(1): Show |
4 | HG03130.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+9517G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539807 | |||||||
chr19:29539809 | T | G | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0196 others(1): Show |
4 | HG03130.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+9519T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539809 | |||||||
chr19:29539833 | G | A | 20 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(17): Show |
23 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.769+9543G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539833 | |||||||
chr19:29539834 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.769+9544C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539834 | |||||||
chr19:29539860 | C | T | 1 | a0001c0001t0001g0235 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.769+9570C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539860 | |||||||
chr19:29539927 | C | A | 2 | a0001c0001t0001g0017 a0007c0010t0001g0149 |
3 | HG04184.hp1 NA18966.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.769+9637C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539927 | |||||||
chr19:29539977 | C | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0196 others(1): Show |
4 | HG03130.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+9687C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29539977 | |||||||
chr19:29540223 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.769+9933A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540223 | |||||||
chr19:29540269 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.769+9979C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540269 | |||||||
chr19:29540302 | C | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+10012C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540302 | |||||||
chr19:29540382 | G | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+10092G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540382 | |||||||
chr19:29540517 | G | C | 1 | a0001c0001t0001g0277 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.769+10227G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540517 | |||||||
chr19:29540524 | C | T | 1 | a0001c0001t0001g0234 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.769+10234C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540524 | |||||||
chr19:29540600 | C | G | 2 | a0001c0001t0001g0083 a0001c0001t0001g0084 |
2 | HG01884.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.769+10310C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540600 | |||||||
chr19:29540623 | A | G | 11 | a0001c0001t0001g0103 a0001c0001t0001g0354 a0001c0001t0004g0155 others(8): Show |
12 | HG02040.hp1 HG02257.hp2 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.769+10333A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29540623 | |||||||
chr19:29541065 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+10775T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541065 | |||||||
chr19:29541175 | T | C | 1 | a0001c0004t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.769+10885T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541175 | |||||||
chr19:29541184 | T | A | 1 | a0001c0001t0001g0134 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.769+10894T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541184 | |||||||
chr19:29541345 | A | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11055A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541345 | |||||||
chr19:29541456 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11166A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541456 | |||||||
chr19:29541497 | G | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11207G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541497 | |||||||
chr19:29541622 | G | A | 18 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(15): Show |
20 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(17): Show |
intron_variant | MODIFIER | c.769+11332G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541622 | |||||||
chr19:29541908 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.769+11618C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29541908 | |||||||
chr19:29542132 | T | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11842T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542132 | |||||||
chr19:29542135 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11845A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542135 | |||||||
chr19:29542137 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11847A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542137 | |||||||
chr19:29542213 | T | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+11923T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542213 | |||||||
chr19:29542328 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.769+12038T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542328 | |||||||
chr19:29542340 | T | C | 4 | a0001c0003t0001g0012 a0001c0003t0001g0057 a0001c0003t0001g0059 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+12050T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542340 | |||||||
chr19:29542591 | G | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+12301G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542591 | |||||||
chr19:29542616 | G | C | 1 | a0001c0003t0001g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.769+12326G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542616 | |||||||
chr19:29542652 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+12362G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542652 | |||||||
chr19:29542652 | G | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0308 a0001c0001t0001g0309 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+12362G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542652 | |||||||
chr19:29542832 | T | C | 8 | a0001c0001t0001g0024 a0001c0001t0001g0068 a0001c0001t0001g0076 others(5): Show |
10 | HG02258.hp2 HG02486.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.769+12542T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542832 | |||||||
chr19:29542873 | G | A | 4 | a0001c0001t0001g0036 a0001c0001t0001g0308 a0001c0001t0001g0309 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+12583G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29542873 | |||||||
chr19:29543026 | A | T | 13 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(10): Show |
15 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.769+12736A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543026 | |||||||
chr19:29543175 | A | T | 2 | a0001c0004t0001g0200 a0001c0004t0002g0199 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.769+12885A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543175 | |||||||
chr19:29543395 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0196 others(1): Show |
4 | HG03130.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+13105G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543395 | |||||||
chr19:29543397 | G | A | 19 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
20 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+13107G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543397 | |||||||
chr19:29543469 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.769+13179G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543469 | |||||||
chr19:29543512 | G | A | 5 | a0001c0001t0001g0014 a0001c0001t0001g0101 a0001c0001t0001g0102 others(2): Show |
6 | HG01884.hp2 HG02809.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+13222G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543512 | |||||||
chr19:29543517 | G | A | 1 | a0001c0001t0001g0103 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.769+13227G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543517 | |||||||
chr19:29543610 | G | A | 2 | a0001c0004t0001g0200 a0001c0004t0002g0199 |
2 | NA20752.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.769+13320G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543610 | |||||||
chr19:29543779 | T | C | 7 | a0001c0001t0001g0067 a0001c0001t0001g0077 a0001c0001t0001g0078 others(4): Show |
7 | HG01884.hp1 HG02055.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+13489T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543779 | |||||||
chr19:29543786 | G | A | 19 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
20 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+13496G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543786 | |||||||
chr19:29543912 | C | T | 2 | a0001c0001t0001g0175 a0001c0001t0001g0176 |
2 | NA18963.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.769+13622C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29543912 | |||||||
chr19:29544070 | GA | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(9): Show |
14 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.769+13781delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544070 | |||||||
chr19:29544096 | C | G | 1 | a0001c0001t0001g0239 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.769+13806C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544096 | |||||||
chr19:29544115 | C | CTA | 18 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(15): Show |
20 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.769+13839_769+1384 others(6): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544115 | ||||||
chr19:29544200 | C | G | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.769+13910C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544200 | |||||||
chr19:29544301 | C | T | 7 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(4): Show |
7 | HG01891.hp2 HG02109.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.769+14011C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544301 | |||||||
chr19:29544302 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0196 others(1): Show |
4 | HG03130.hp2 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.769+14012G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544302 | |||||||
chr19:29544322 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(9): Show |
14 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.769+14032C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544322 | |||||||
chr19:29544383 | G | A | 1 | a0002c0002t0001g0249 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.769+14093G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544383 | |||||||
chr19:29544384 | G | T | 19 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
20 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+14094G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544384 | |||||||
chr19:29544407 | T | G | 1 | a0001c0004t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.769+14117T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544407 | |||||||
chr19:29544505 | G | A | 2 | a0001c0001t0001g0278 a0002c0002t0002g0312 |
2 | HG02615.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.769+14215G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544505 | |||||||
chr19:29544513 | G | A | 2 | a0001c0001t0001g0180 a0001c0003t0001g0060 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.769+14223G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544513 | |||||||
chr19:29544525 | C | CA | 18 | a0001c0001t0001g0098 a0001c0001t0001g0112 a0001c0001t0001g0113 others(15): Show |
18 | HG00733.hp2 HG01891.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.769+14266dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | C | CAA | 13 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0096 others(10): Show |
13 | HG00642.hp2 HG02015.hp2 HG02165.hp1 others(10): Show |
intron_variant | MODIFIER | c.769+14265_769+1426 others(6): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | C | CAAA | 8 | a0001c0001t0001g0260 a0001c0003t0001g0011 a0001c0003t0001g0043 others(5): Show |
9 | HG00423.hp2 HG00609.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.769+14264_769+1426 others(7): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | CA | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(95): Show |
116 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.769+14266delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | CAA | C | 43 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0068 others(40): Show |
50 | HG00639.hp2 HG00673.hp1 HG00738.hp1 others(47): Show |
intron_variant | MODIFIER | c.769+14265_769+1426 others(6): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | CAAA | C | 93 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0023 others(90): Show |
104 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.769+14264_769+1426 others(7): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | CAAAA | C | 10 | a0001c0001t0001g0007 a0001c0001t0001g0087 a0001c0001t0001g0147 others(7): Show |
12 | HG01069.hp1 HG01256.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.769+14263_769+1426 others(8): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544525 | CAAAAAAA others(3): Show |
C | 10 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(7): Show |
12 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.769+14257_769+1426 others(14): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29544525 | ||||||
chr19:29544558 | T | C | 19 | a0001c0001t0001g0061 a0001c0001t0001g0095 a0001c0001t0001g0096 others(16): Show |
20 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(17): Show |
intron_variant | MODIFIER | c.769+14268T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544558 | |||||||
chr19:29544679 | T | C | 2 | a0001c0001t0001g0257 a0001c0001t0001g0258 |
2 | HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.769+14389T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544679 | |||||||
chr19:29544722 | G | A | 1 | a0002c0002t0001g0264 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.769+14432G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544722 | |||||||
chr19:29544729 | C | T | 1 | a0001c0001t0001g0278 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.769+14439C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544729 | |||||||
chr19:29544982 | G | A | 3 | a0001c0001t0001g0068 a0001c0001t0001g0076 a0001c0001t0001g0104 |
3 | HG02258.hp2 HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.769+14692G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29544982 | |||||||
chr19:29545110 | A | G | 26 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0017 others(23): Show |
33 | HG01255.hp1 HG01361.hp1 HG01943.hp1 others(30): Show |
intron_variant | MODIFIER | c.769+14820A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545110 | |||||||
chr19:29545116 | G | A | 5 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 others(2): Show |
5 | HG02615.hp2 HG02970.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.769+14826G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545116 | |||||||
chr19:29545224 | G | A | 1 | a0001c0001t0001g0077 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.769+14934G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545224 | |||||||
chr19:29545251 | G | A | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG00735.hp2 HG01069.hp1 |
intron_variant | MODIFIER | c.769+14961G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545251 | |||||||
chr19:29545341 | G | A | 11 | a0001c0001t0001g0014 a0001c0001t0001g0101 a0001c0001t0001g0102 others(8): Show |
13 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.769+15051G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545341 | |||||||
chr19:29545515 | A | T | 1 | a0001c0004t0001g0200 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.769+15225A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545515 | |||||||
chr19:29545591 | C | T | 3 | a0001c0001t0004g0155 a0001c0004t0001g0193 a0001c0004t0003g0194 |
3 | HG02818.hp2 HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.769+15301C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545591 | |||||||
chr19:29545662 | G | T | 3 | a0001c0001t0001g0203 a0001c0001t0001g0208 a0002c0002t0001g0338 |
3 | HG01074.hp1 HG01192.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.769+15372G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545662 | |||||||
chr19:29545667 | T | G | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.769+15377T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545667 | |||||||
chr19:29545756 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.769+15466T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545756 | |||||||
chr19:29545870 | GAAAGAAA others(3): Show |
G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0354 a0001c0004t0001g0074 others(1): Show |
4 | HG02040.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+15594_769+1560 others(14): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29545870 | ||||||
chr19:29545884 | G | GA | 4 | a0001c0003t0001g0012 a0001c0003t0001g0057 a0001c0003t0001g0059 others(1): Show |
5 | HG02257.hp2 HG02895.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.769+15598dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29545884 | ||||||
chr19:29545993 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.769+15703G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29545993 | |||||||
chr19:29546049 | G | A | 1 | a0001c0003t0001g0056 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.769+15759G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546049 | |||||||
chr19:29546102 | T | G | 4 | a0001c0001t0001g0103 a0001c0001t0001g0354 a0001c0004t0001g0074 others(1): Show |
4 | HG02040.hp1 HG03453.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+15812T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546102 | |||||||
chr19:29546140 | G | A | 2 | a0001c0001t0001g0180 a0001c0003t0001g0060 |
2 | HG02717.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.769+15850G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546140 | |||||||
chr19:29546174 | A | G | 150 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0020 others(147): Show |
171 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.769+15884A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546174 | |||||||
chr19:29546307 | G | A | 5 | a0001c0001t0001g0019 a0001c0001t0001g0123 a0001c0001t0001g0124 others(2): Show |
6 | NA18981.hp2 NA19005.hp1 NA19011.hp2 others(3): Show |
intron_variant | MODIFIER | c.769+16017G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546307 | |||||||
chr19:29546344 | A | G | 1 | a0001c0001t0001g0016 | 2 | HG00639.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.769+16054A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546344 | |||||||
chr19:29546402 | C | T | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0093 others(1): Show |
4 | HG00673.hp2 NA18959.hp1 NA18995.hp1 others(1): Show |
intron_variant | MODIFIER | c.769+16112C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546402 | |||||||
chr19:29546456 | G | GA | 21 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(18): Show |
23 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.769+16168dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29546456 | ||||||
chr19:29546459 | C | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(18): Show |
23 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.769+16169C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546459 | |||||||
chr19:29546494 | A | G | 2 | a0002c0002t0001g0313 a0002c0002t0001g0320 |
2 | HG00438.hp1 NA18954.hp2 |
intron_variant | MODIFIER | c.769+16204A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546494 | |||||||
chr19:29546496 | A | G | 21 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(18): Show |
23 | HG00741.hp2 HG01256.hp1 HG01258.hp2 others(20): Show |
intron_variant | MODIFIER | c.769+16206A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546496 | |||||||
chr19:29546526 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.769+16236C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546526 | |||||||
chr19:29546584 | G | C | 8 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(5): Show |
8 | HG00741.hp2 HG01891.hp2 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.769+16294G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546584 | |||||||
chr19:29546652 | C | T | 3 | a0001c0001t0001g0214 a0001c0001t0001g0231 a0001c0001t0001g0244 |
3 | HG01255.hp2 HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.769+16362C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546652 | |||||||
chr19:29546655 | C | T | 7 | a0001c0001t0001g0273 a0001c0003t0001g0011 a0001c0003t0001g0040 others(4): Show |
8 | HG00423.hp2 HG00558.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.769+16365C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546655 | |||||||
chr19:29546670 | G | GC | 16 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(13): Show |
18 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.769+16385dupC | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29546670 | ||||||
chr19:29546676 | A | C | 27 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(24): Show |
30 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.769+16386A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546676 | |||||||
chr19:29546681 | C | T | 1 | a0001c0003t0001g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.769+16391C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546681 | |||||||
chr19:29546687 | G | C | 1 | a0001c0001t0001g0309 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.769+16397G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546687 | |||||||
chr19:29546703 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0173 |
3 | HG02257.hp1 HG02280.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.769+16413G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546703 | |||||||
chr19:29546968 | G | C | 13 | a0001c0001t0001g0036 a0001c0001t0001g0067 a0001c0001t0001g0077 others(10): Show |
14 | HG01167.hp2 HG01169.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.769+16678G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29546968 | |||||||
chr19:29547056 | T | C | 8 | a0001c0001t0001g0014 a0001c0001t0001g0089 a0001c0001t0001g0101 others(5): Show |
10 | HG01256.hp1 HG01258.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.769+16766T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547056 | |||||||
chr19:29547075 | C | G | 6 | a0001c0001t0001g0257 a0001c0001t0001g0258 a0001c0001t0001g0259 others(3): Show |
6 | HG00741.hp2 HG01891.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.770-16771C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547075 | |||||||
chr19:29547116 | A | C | 20 | a0001c0001t0001g0029 a0001c0001t0001g0070 a0001c0001t0001g0071 others(17): Show |
21 | HG01081.hp2 HG01496.hp1 HG01891.hp1 others(18): Show |
intron_variant | MODIFIER | c.770-16730A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547116 | |||||||
chr19:29547172 | T | C | 7 | a0001c0001t0001g0273 a0001c0003t0001g0011 a0001c0003t0001g0040 others(4): Show |
8 | HG00423.hp2 HG00558.hp1 NA18939.hp2 others(5): Show |
intron_variant | MODIFIER | c.770-16674T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547172 | |||||||
chr19:29547510 | G | A | 1 | a0001c0003t0001g0013 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.770-16336G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547510 | |||||||
chr19:29547514 | A | G | 1 | a0001c0004t0001g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770-16332A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547514 | |||||||
chr19:29547574 | G | A | 1 | a0002c0002t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.770-16272G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547574 | |||||||
chr19:29547596 | A | T | 1 | a0002c0002t0001g0314 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.770-16250A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547596 | |||||||
chr19:29547737 | T | C | 1 | a0001c0001t0001g0073 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.770-16109T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547737 | |||||||
chr19:29547778 | G | A | 4 | a0001c0001t0001g0180 a0001c0003t0001g0060 a0001c0004t0001g0193 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-16068G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547778 | |||||||
chr19:29547817 | C | T | 2 | a0001c0001t0001g0146 a0001c0003t0001g0056 |
2 | HG00741.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.770-16029C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547817 | |||||||
chr19:29547832 | T | C | 1 | a0001c0001t0001g0120 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.770-16014T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547832 | |||||||
chr19:29547865 | G | T | 4 | a0001c0001t0001g0180 a0001c0003t0001g0060 a0001c0004t0001g0193 others(1): Show |
4 | HG02717.hp2 HG02896.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-15981G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547865 | |||||||
chr19:29547906 | C | T | 1 | a0001c0001t0001g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.770-15940C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547906 | |||||||
chr19:29547981 | T | C | 128 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0024 others(125): Show |
140 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(137): Show |
intron_variant | MODIFIER | c.770-15865T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29547981 | |||||||
chr19:29548037 | A | G | 1 | a0001c0001t0001g0290 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.770-15809A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548037 | |||||||
chr19:29548046 | T | A | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.770-15800T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548046 | |||||||
chr19:29548054 | A | C | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.770-15792A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548054 | |||||||
chr19:29548055 | C | A | 1 | a0001c0001t0001g0119 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.770-15791C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548055 | |||||||
chr19:29548240 | C | T | 3 | a0001c0003t0001g0012 a0001c0003t0001g0056 a0001c0003t0001g0059 |
4 | HG00741.hp2 HG02257.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-15606C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548240 | |||||||
chr19:29548323 | C | G | 3 | a0001c0003t0001g0012 a0001c0003t0001g0056 a0001c0003t0001g0059 |
4 | HG00741.hp2 HG02257.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-15523C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548323 | |||||||
chr19:29548426 | C | T | 1 | a0001c0001t0001g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.770-15420C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548426 | |||||||
chr19:29548582 | A | T | 1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.770-15264A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548582 | |||||||
chr19:29548626 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.770-15220C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548626 | |||||||
chr19:29548685 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0133 a0001c0001t0001g0198 others(5): Show |
9 | HG00639.hp2 HG02109.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.770-15161C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548685 | |||||||
chr19:29548725 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0118 |
3 | HG00140.hp1 HG00733.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.770-15121C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548725 | |||||||
chr19:29548890 | G | C | 18 | a0001c0001t0001g0096 a0001c0001t0001g0273 a0001c0001t0001g0289 others(15): Show |
19 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(16): Show |
intron_variant | MODIFIER | c.770-14956G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29548890 | |||||||
chr19:29549194 | C | T | 1 | a0002c0002t0001g0337 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.770-14652C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549194 | |||||||
chr19:29549263 | T | G | 1 | a0002c0002t0002g0315 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.770-14583T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549263 | |||||||
chr19:29549414 | G | T | 2 | a0001c0003t0003g0058 a0004c0007t0001g0064 |
2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.770-14432G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549414 | |||||||
chr19:29549465 | C | T | 25 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0096 others(22): Show |
26 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-14381C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549465 | |||||||
chr19:29549512 | A | ACTGCCCC others(27): Show |
1 | a0001c0001t0001g0067 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.770-14322_770-1432 others(38): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29549512 | ||||||
chr19:29549512 | A | ACTGCCCC others(27): Show |
228 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(225): Show |
256 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(253): Show |
intron_variant | MODIFIER | c.770-14322_770-1432 others(38): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29549512 | ||||||
chr19:29549512 | A | ACTGCCCC others(27): Show |
33 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(30): Show |
39 | HG00639.hp2 HG00741.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.770-14322_770-1432 others(38): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29549512 | ||||||
chr19:29549558 | G | C | 2 | a0001c0003t0001g0012 a0001c0003t0001g0059 |
3 | HG02257.hp2 HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.770-14288G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549558 | |||||||
chr19:29549578 | A | G | 94 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(91): Show |
104 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.770-14268A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549578 | |||||||
chr19:29549654 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0279 |
2 | HG02165.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.770-14192C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549654 | |||||||
chr19:29549705 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0279 |
2 | HG02165.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.770-14141G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549705 | |||||||
chr19:29549720 | G | A | 1 | a0001c0001t0001g0261 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.770-14126G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549720 | |||||||
chr19:29549864 | C | T | 22 | a0001c0001t0001g0016 a0001c0001t0001g0078 a0001c0001t0001g0079 others(19): Show |
25 | HG00639.hp2 HG00741.hp2 HG02040.hp1 others(22): Show |
intron_variant | MODIFIER | c.770-13982C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549864 | |||||||
chr19:29549929 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.770-13917G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29549929 | |||||||
chr19:29550051 | G | T | 2 | a0001c0001t0001g0097 a0001c0001t0001g0135 |
2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.770-13795G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550051 | |||||||
chr19:29550119 | A | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(167): Show |
194 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.770-13727A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550119 | |||||||
chr19:29550179 | A | G | 1 | a0001c0004t0001g0201 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.770-13667A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550179 | |||||||
chr19:29550204 | C | T | 1 | a0001c0003t0001g0047 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.770-13642C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550204 | |||||||
chr19:29550205 | G | A | 2 | a0001c0001t0001g0220 a0001c0001t0001g0274 |
2 | HG04184.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.770-13641G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550205 | |||||||
chr19:29550231 | G | C | 2 | a0001c0001t0001g0280 a0002c0002t0001g0292 |
2 | NA18955.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.770-13615G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550231 | |||||||
chr19:29550237 | T | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(258): Show |
295 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(292): Show |
intron_variant | MODIFIER | c.770-13609T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550237 | |||||||
chr19:29550338 | G | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(166): Show |
193 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.770-13508G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550338 | |||||||
chr19:29550434 | A | G | 9 | a0001c0001t0001g0142 a0001c0001t0001g0280 a0002c0002t0001g0002 others(6): Show |
15 | HG00423.hp1 HG00639.hp1 HG01074.hp2 others(12): Show |
intron_variant | MODIFIER | c.770-13412A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550434 | |||||||
chr19:29550472 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.770-13374T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550472 | |||||||
chr19:29550597 | G | A | 4 | a0001c0001t0001g0114 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG01943.hp2 HG01993.hp2 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-13249G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550597 | |||||||
chr19:29550630 | G | A | 1 | a0001c0003t0001g0059 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.770-13216G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550630 | |||||||
chr19:29550646 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(266): Show |
303 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(300): Show |
intron_variant | MODIFIER | c.770-13200G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550646 | |||||||
chr19:29550727 | C | T | 91 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(88): Show |
101 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(98): Show |
intron_variant | MODIFIER | c.770-13119C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550727 | |||||||
chr19:29550761 | G | C | 1 | a0001c0001t0001g0005 | 3 | NA18962.hp2 NA18988.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.770-13085G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550761 | |||||||
chr19:29550829 | G | GA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0077 others(10): Show |
16 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(13): Show |
intron_variant | MODIFIER | c.770-13004dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29550829 | ||||||
chr19:29550829 | G | GAA | 16 | a0001c0001t0001g0096 a0001c0001t0001g0273 a0001c0001t0001g0289 others(13): Show |
17 | HG00423.hp2 HG00544.hp2 HG00558.hp1 others(14): Show |
intron_variant | MODIFIER | c.770-13005_770-1300 others(6): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29550829 | ||||||
chr19:29550829 | GA | G | 67 | a0001c0001t0001g0068 a0001c0001t0001g0070 a0001c0001t0001g0071 others(64): Show |
71 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.770-13004delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29550829 | ||||||
chr19:29550861 | C | A | 1 | a0001c0001t0001g0207 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.770-12985C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550861 | |||||||
chr19:29550889 | A | T | 1 | a0001c0001t0009g0355 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.770-12957A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550889 | |||||||
chr19:29550918 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(165): Show |
192 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.770-12928G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550918 | |||||||
chr19:29550946 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(257): Show |
294 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(291): Show |
intron_variant | MODIFIER | c.770-12900T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550946 | |||||||
chr19:29550955 | C | T | 10 | a0001c0001t0001g0007 a0001c0001t0001g0020 a0001c0001t0001g0021 others(7): Show |
14 | HG00735.hp2 HG01069.hp1 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-12891C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550955 | |||||||
chr19:29550976 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.770-12870C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29550976 | |||||||
chr19:29551046 | A | G | 21 | a0001c0001t0001g0016 a0001c0001t0001g0078 a0001c0001t0001g0079 others(18): Show |
24 | HG00639.hp2 HG00741.hp2 HG02040.hp1 others(21): Show |
intron_variant | MODIFIER | c.770-12800A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551046 | |||||||
chr19:29551083 | C | G | 1 | a0001c0001t0001g0078 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.770-12763C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551083 | |||||||
chr19:29551421 | C | G | 59 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(56): Show |
62 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(59): Show |
intron_variant | MODIFIER | c.770-12425C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551421 | |||||||
chr19:29551480 | A | T | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770-12366A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551480 | |||||||
chr19:29551481 | G | A | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770-12365G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551481 | |||||||
chr19:29551490 | G | A | 2 | a0001c0001t0001g0180 a0001c0004t0001g0193 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770-12356G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551490 | |||||||
chr19:29551828 | T | A | 1 | a0001c0003t0001g0052 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.770-12018T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551828 | |||||||
chr19:29551851 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-11995G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29551851 | |||||||
chr19:29552006 | A | C | 33 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(30): Show |
38 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(35): Show |
intron_variant | MODIFIER | c.770-11840A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552006 | |||||||
chr19:29552231 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-11615C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552231 | |||||||
chr19:29552261 | A | G | 2 | a0001c0004t0001g0191 a0001c0004t0001g0192 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.770-11585A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552261 | |||||||
chr19:29552285 | A | T | 24 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0209 others(21): Show |
31 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.770-11561A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552285 | |||||||
chr19:29552315 | A | G | 114 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0067 others(111): Show |
129 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.770-11531A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552315 | |||||||
chr19:29552375 | A | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-11471A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552375 | |||||||
chr19:29552400 | G | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-11446G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552400 | |||||||
chr19:29552403 | G | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-11443G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552403 | |||||||
chr19:29552565 | T | C | 26 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(23): Show |
30 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.770-11281T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552565 | |||||||
chr19:29552594 | C | T | 2 | a0001c0001t0001g0180 a0001c0004t0001g0193 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770-11252C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552594 | |||||||
chr19:29552654 | T | A | 1 | a0001c0004t0001g0066 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.770-11192T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552654 | |||||||
chr19:29552710 | G | A | 1 | a0001c0003t0001g0043 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.770-11136G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552710 | |||||||
chr19:29552978 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-10868C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552978 | |||||||
chr19:29552983 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
325 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.770-10863A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29552983 | |||||||
chr19:29553041 | C | G | 24 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0209 others(21): Show |
31 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.770-10805C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553041 | |||||||
chr19:29553131 | G | GCAGTAC | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-10712_770-1071 others(10): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29553131 | ||||||
chr19:29553176 | C | CCATACAC others(2): Show |
24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-10664_770-1066 others(13): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29553176 | ||||||
chr19:29553265 | C | A | 16 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(13): Show |
20 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.770-10581C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553265 | |||||||
chr19:29553300 | A | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0147 |
3 | HG02155.hp1 NA19065.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.770-10546A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553300 | |||||||
chr19:29553309 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-10537A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553309 | |||||||
chr19:29553362 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-10484C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553362 | |||||||
chr19:29553377 | A | G | 1 | a0001c0001t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.770-10469A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553377 | |||||||
chr19:29553386 | G | A | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
325 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(322): Show |
intron_variant | MODIFIER | c.770-10460G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553386 | |||||||
chr19:29553512 | G | A | 128 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(125): Show |
144 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.770-10334G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553512 | |||||||
chr19:29553565 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.770-10281A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553565 | |||||||
chr19:29553581 | A | G | 1 | a0001c0001t0001g0224 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.770-10265A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553581 | |||||||
chr19:29553807 | T | C | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-10039T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553807 | |||||||
chr19:29553863 | A | C | 344 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(341): Show |
391 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(388): Show |
intron_variant | MODIFIER | c.770-9983A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553863 | |||||||
chr19:29553868 | TA | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
12 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-9977delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553868 | |||||||
chr19:29553882 | T | G | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-9964T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553882 | |||||||
chr19:29553998 | C | T | 1 | a0001c0001t0001g0270 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.770-9848C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29553998 | |||||||
chr19:29554017 | A | G | 66 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(63): Show |
70 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(67): Show |
intron_variant | MODIFIER | c.770-9829A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554017 | |||||||
chr19:29554031 | C | G | 1 | a0001c0001t0005g0256 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.770-9815C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554031 | |||||||
chr19:29554037 | A | C | 9 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
10 | HG02055.hp1 HG02615.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-9809A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554037 | |||||||
chr19:29554079 | G | T | 1 | a0002c0002t0002g0325 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.770-9767G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554079 | |||||||
chr19:29554265 | A | G | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-9581A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554265 | |||||||
chr19:29554307 | A | G | 1 | a0001c0001t0001g0171 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.770-9539A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554307 | |||||||
chr19:29554376 | A | C | 14 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-9470A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554376 | |||||||
chr19:29554380 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-9466A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554380 | |||||||
chr19:29554600 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.770-9246C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554600 | |||||||
chr19:29554620 | A | C | 17 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(14): Show |
21 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.770-9226A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554620 | |||||||
chr19:29554626 | G | A | 128 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(125): Show |
144 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.770-9220G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554626 | |||||||
chr19:29554683 | C | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(19): Show |
26 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-9163C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554683 | |||||||
chr19:29554693 | C | T | 6 | a0001c0001t0001g0286 a0001c0003t0001g0011 a0001c0003t0001g0040 others(3): Show |
7 | NA18939.hp2 NA18940.hp2 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-9153C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554693 | |||||||
chr19:29554812 | G | A | 1 | a0001c0001t0001g0141 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.770-9034G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554812 | |||||||
chr19:29554823 | T | C | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.770-9023T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554823 | |||||||
chr19:29554941 | C | T | 2 | a0001c0001t0001g0341 a0001c0001t0001g0342 |
2 | HG02572.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.770-8905C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554941 | |||||||
chr19:29554950 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-8896C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554950 | |||||||
chr19:29554955 | C | T | 1 | a0001c0001t0001g0260 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.770-8891C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554955 | |||||||
chr19:29554972 | T | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0197 others(4): Show |
7 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-8874T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29554972 | |||||||
chr19:29555021 | G | A | 2 | a0001c0001t0001g0018 a0001c0001t0001g0118 |
3 | HG00140.hp1 HG00733.hp1 HG01123.hp1 |
intron_variant | MODIFIER | c.770-8825G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555021 | |||||||
chr19:29555075 | C | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-8771C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555075 | |||||||
chr19:29555087 | C | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0262 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-8759C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555087 | |||||||
chr19:29555268 | C | T | 12 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(9): Show |
13 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-8578C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555268 | |||||||
chr19:29555330 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-8516A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555330 | |||||||
chr19:29555519 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.770-8327C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555519 | |||||||
chr19:29555639 | T | A | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-8207T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555639 | |||||||
chr19:29555647 | ATAGT | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-8195_770-8192d others(6): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29555647 | ||||||
chr19:29555723 | G | A | 14 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-8123G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555723 | |||||||
chr19:29555728 | C | T | 1 | a0001c0001t0012g0232 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.770-8118C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555728 | |||||||
chr19:29555850 | T | C | 1 | a0002c0002t0001g0350 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.770-7996T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555850 | |||||||
chr19:29555926 | A | G | 1 | a0001c0003t0001g0042 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.770-7920A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555926 | |||||||
chr19:29555972 | T | C | 128 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(125): Show |
144 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.770-7874T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29555972 | |||||||
chr19:29556016 | C | T | 24 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0209 others(21): Show |
31 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.770-7830C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556016 | |||||||
chr19:29556099 | C | CA | 136 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(133): Show |
159 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.770-7734dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29556099 | ||||||
chr19:29556099 | CA | C | 34 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(31): Show |
39 | HG00558.hp1 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.770-7734delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29556099 | ||||||
chr19:29556107 | A | G | 10 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
12 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-7739A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556107 | |||||||
chr19:29556108 | A | G | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-7738A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556108 | |||||||
chr19:29556139 | T | C | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0262 others(2): Show |
5 | HG02280.hp2 HG02717.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-7707T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556139 | |||||||
chr19:29556150 | GA | G | 22 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(19): Show |
26 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-7695delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556150 | |||||||
chr19:29556225 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
12 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-7621G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556225 | |||||||
chr19:29556236 | T | C | 105 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(102): Show |
114 | HG00323.hp2 HG00544.hp1 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.770-7610T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556236 | |||||||
chr19:29556237 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(14): Show |
21 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.770-7609C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556237 | |||||||
chr19:29556247 | A | G | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-7599A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556247 | |||||||
chr19:29556271 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.770-7575G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556271 | |||||||
chr19:29556288 | T | C | 56 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(53): Show |
59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.770-7558T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556288 | |||||||
chr19:29556319 | C | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
12 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-7527C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556319 | |||||||
chr19:29556355 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(14): Show |
21 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.770-7491C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556355 | |||||||
chr19:29556379 | A | G | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-7467A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556379 | |||||||
chr19:29556382 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.770-7464C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556382 | |||||||
chr19:29556401 | G | A | 2 | a0001c0001t0001g0289 a0002c0002t0001g0321 |
2 | NA18986.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.770-7445G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556401 | |||||||
chr19:29556413 | C | A | 17 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(14): Show |
21 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.770-7433C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556413 | |||||||
chr19:29556522 | G | A | 1 | a0001c0001t0002g0227 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.770-7324G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556522 | |||||||
chr19:29556527 | T | C | 2 | a0001c0001t0001g0207 a0001c0004t0001g0201 |
2 | HG04228.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.770-7319T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556527 | |||||||
chr19:29556580 | G | C | 1 | a0001c0004t0001g0191 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.770-7266G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556580 | |||||||
chr19:29556591 | A | ACTGTGT | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-7251_770-7250i others(8): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29556591 | ||||||
chr19:29556648 | G | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0003g0085 others(1): Show |
4 | HG02717.hp2 HG03130.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-7198G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556648 | |||||||
chr19:29556739 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.770-7107T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556739 | |||||||
chr19:29556898 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.770-6948G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556898 | |||||||
chr19:29556980 | G | T | 22 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(19): Show |
26 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.770-6866G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29556980 | |||||||
chr19:29557022 | T | TA | 5 | a0001c0001t0001g0006 a0001c0001t0001g0214 a0001c0001t0001g0228 others(2): Show |
7 | HG01109.hp2 HG01255.hp2 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-6816dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29557022 | ||||||
chr19:29557161 | A | ATGGTACA others(5): Show |
9 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
10 | HG02055.hp1 HG02615.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-6682_770-6671d others(14): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29557161 | ||||||
chr19:29557235 | C | T | 56 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(53): Show |
59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.770-6611C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557235 | |||||||
chr19:29557296 | T | A | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-6550T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557296 | |||||||
chr19:29557319 | G | T | 1 | a0001c0004t0001g0074 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.770-6527G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557319 | |||||||
chr19:29557403 | A | G | 1 | a0001c0001t0001g0262 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.770-6443A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557403 | |||||||
chr19:29557492 | G | A | 1 | a0002c0002t0001g0035 | 2 | NA18952.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.770-6354G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557492 | |||||||
chr19:29557519 | G | GA | 3 | a0001c0001t0001g0024 a0001c0001t0001g0089 a0001c0001t0001g0354 |
4 | HG02109.hp2 HG02922.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.770-6324dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29557519 | ||||||
chr19:29557544 | A | G | 1 | a0001c0003t0013g0045 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.770-6302A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557544 | |||||||
chr19:29557555 | T | C | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-6291T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557555 | |||||||
chr19:29557614 | G | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-6232G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557614 | |||||||
chr19:29557654 | G | A | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-6192G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557654 | |||||||
chr19:29557671 | C | A | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-6175C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557671 | |||||||
chr19:29557699 | C | CA | 13 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(10): Show |
14 | HG02040.hp1 HG02055.hp1 HG02074.hp1 others(11): Show |
intron_variant | MODIFIER | c.770-6133dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29557699 | ||||||
chr19:29557699 | CA | C | 57 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(54): Show |
60 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.770-6133delA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29557699 | ||||||
chr19:29557814 | C | T | 23 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(20): Show |
27 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.770-6032C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557814 | |||||||
chr19:29557884 | A | G | 5 | a0002c0002t0001g0185 a0002c0002t0001g0293 a0002c0002t0001g0345 others(2): Show |
5 | NA18986.hp1 NA18992.hp2 NA18998.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-5962A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557884 | |||||||
chr19:29557955 | C | T | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-5891C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557955 | |||||||
chr19:29557991 | A | G | 56 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(53): Show |
59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.770-5855A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29557991 | |||||||
chr19:29558048 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.770-5798C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558048 | |||||||
chr19:29558087 | G | A | 3 | a0001c0001t0001g0080 a0001c0001t0001g0081 a0001c0001t0001g0082 |
3 | HG02615.hp2 HG02970.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.770-5759G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558087 | |||||||
chr19:29558113 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.770-5733C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558113 | |||||||
chr19:29558171 | C | T | 3 | a0001c0001t0001g0075 a0001c0001t0001g0143 a0002c0002t0001g0318 |
3 | HG02738.hp2 HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.770-5675C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558171 | |||||||
chr19:29558232 | G | A | 2 | a0001c0001t0001g0180 a0001c0004t0001g0193 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770-5614G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558232 | |||||||
chr19:29558413 | G | A | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.770-5433G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558413 | |||||||
chr19:29558440 | G | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0102 others(7): Show |
13 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-5406G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558440 | |||||||
chr19:29558464 | C | T | 4 | a0001c0001t0001g0290 a0001c0001t0001g0324 a0001c0001t0001g0340 others(1): Show |
4 | HG01123.hp2 HG02717.hp1 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-5382C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558464 | |||||||
chr19:29558465 | G | A | 1 | a0001c0001t0001g0139 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.770-5381G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558465 | |||||||
chr19:29558491 | A | C | 143 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(140): Show |
166 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.770-5355A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558491 | |||||||
chr19:29558496 | G | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-5350G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558496 | |||||||
chr19:29558560 | C | G | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-5286C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558560 | |||||||
chr19:29558584 | A | G | 1 | a0001c0003t0001g0053 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.770-5262A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558584 | |||||||
chr19:29558627 | A | G | 56 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(53): Show |
59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.770-5219A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558627 | |||||||
chr19:29558659 | A | C | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-5187A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558659 | |||||||
chr19:29558726 | G | A | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-5120G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558726 | |||||||
chr19:29558873 | T | A | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-4973T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558873 | |||||||
chr19:29558966 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.770-4880A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29558966 | |||||||
chr19:29559061 | T | A | 1 | a0001c0001t0001g0173 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.770-4785T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559061 | |||||||
chr19:29559131 | T | C | 1 | a0001c0001t0001g0082 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.770-4715T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559131 | |||||||
chr19:29559192 | G | A | 2 | a0001c0001t0001g0132 a0001c0004t0001g0074 |
2 | HG02040.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.770-4654G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559192 | |||||||
chr19:29559262 | C | G | 24 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0209 others(21): Show |
31 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.770-4584C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559262 | |||||||
chr19:29559300 | T | C | 1 | a0001c0001t0001g0036 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.770-4546T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559300 | |||||||
chr19:29559304 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0180 a0001c0001t0001g0198 others(5): Show |
9 | HG00323.hp2 HG00639.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.770-4542C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559304 | |||||||
chr19:29559316 | A | G | 56 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(53): Show |
59 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.770-4530A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559316 | |||||||
chr19:29559345 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.770-4501G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559345 | |||||||
chr19:29559346 | C | T | 17 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(14): Show |
21 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(18): Show |
intron_variant | MODIFIER | c.770-4500C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559346 | |||||||
chr19:29559379 | C | T | 15 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(12): Show |
16 | HG00323.hp2 HG00639.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.770-4467C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559379 | |||||||
chr19:29559385 | G | C | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-4461G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559385 | |||||||
chr19:29559428 | G | A | 35 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(32): Show |
43 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.770-4418G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559428 | |||||||
chr19:29559439 | G | A | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-4407G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559439 | |||||||
chr19:29559439 | G | C | 1 | a0002c0002t0002g0322 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.770-4407G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559439 | |||||||
chr19:29559574 | T | C | 25 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(22): Show |
29 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(26): Show |
intron_variant | MODIFIER | c.770-4272T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559574 | |||||||
chr19:29559659 | T | G | 129 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0036 others(126): Show |
145 | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(142): Show |
intron_variant | MODIFIER | c.770-4187T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559659 | |||||||
chr19:29559761 | G | A | 5 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0206 others(2): Show |
5 | HG02717.hp2 HG03130.hp2 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-4085G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559761 | |||||||
chr19:29559793 | T | A | 1 | a0002c0002t0001g0296 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.770-4053T>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559793 | |||||||
chr19:29559983 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.770-3863G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559983 | |||||||
chr19:29559988 | C | T | 1 | a0001c0001t0001g0259 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.770-3858C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29559988 | |||||||
chr19:29560164 | C | T | 24 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(21): Show |
28 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(25): Show |
intron_variant | MODIFIER | c.770-3682C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560164 | |||||||
chr19:29560264 | T | C | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0197 others(4): Show |
7 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-3582T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560264 | |||||||
chr19:29560394 | C | G | 26 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(23): Show |
30 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(27): Show |
intron_variant | MODIFIER | c.770-3452C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560394 | |||||||
chr19:29560460 | A | G | 2 | a0001c0001t0001g0180 a0001c0004t0001g0193 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770-3386A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560460 | |||||||
chr19:29560650 | G | A | 46 | a0001c0001t0001g0067 a0001c0001t0001g0070 a0001c0001t0001g0071 others(43): Show |
49 | HG00544.hp1 HG00558.hp2 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.770-3196G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560650 | |||||||
chr19:29560702 | C | T | 24 | a0001c0001t0001g0096 a0001c0001t0001g0172 a0001c0001t0001g0209 others(21): Show |
31 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(28): Show |
intron_variant | MODIFIER | c.770-3144C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560702 | |||||||
chr19:29560769 | A | G | 1 | a0001c0001t0001g0240 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.770-3077A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560769 | |||||||
chr19:29560839 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.770-3007G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560839 | |||||||
chr19:29560966 | T | C | 18 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(15): Show |
22 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(19): Show |
intron_variant | MODIFIER | c.770-2880T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29560966 | |||||||
chr19:29561041 | A | G | 11 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(8): Show |
13 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-2805A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561041 | |||||||
chr19:29561078 | G | A | 10 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(7): Show |
12 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(9): Show |
intron_variant | MODIFIER | c.770-2768G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561078 | |||||||
chr19:29561093 | C | T | 1 | a0001c0004t0001g0190 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.770-2753C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561093 | |||||||
chr19:29561146 | T | G | 7 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0197 others(4): Show |
7 | HG01891.hp2 HG02630.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.770-2700T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561146 | |||||||
chr19:29561172 | C | G | 1 | a0001c0001t0001g0110 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.770-2674C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561172 | |||||||
chr19:29561181 | A | C | 39 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0036 others(36): Show |
45 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(42): Show |
intron_variant | MODIFIER | c.770-2665A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561181 | |||||||
chr19:29561237 | G | T | 2 | a0001c0001t0001g0180 a0001c0004t0001g0193 |
2 | HG02896.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.770-2609G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561237 | |||||||
chr19:29561298 | T | G | 1 | a0001c0001t0001g0172 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.770-2548T>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561298 | |||||||
chr19:29561311 | C | CA | 9 | a0001c0001t0001g0078 a0001c0001t0001g0080 a0001c0001t0001g0081 others(6): Show |
10 | HG02055.hp1 HG02615.hp2 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.770-2528dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29561311 | ||||||
chr19:29561325 | T | TA | 38 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0036 others(35): Show |
44 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(41): Show |
intron_variant | MODIFIER | c.770-2513dupA | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29561325 | ||||||
chr19:29561331 | A | T | 1 | a0001c0001t0005g0255 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.770-2515A>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561331 | |||||||
chr19:29561389 | C | T | 16 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(13): Show |
17 | HG00323.hp2 HG00639.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-2457C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561389 | |||||||
chr19:29561411 | G | A | 1 | a0002c0002t0001g0313 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.770-2435G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561411 | |||||||
chr19:29561467 | C | T | 353 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(350): Show |
402 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(399): Show |
intron_variant | MODIFIER | c.770-2379C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561467 | |||||||
chr19:29561566 | A | G | 3 | a0001c0001t0001g0079 a0001c0001t0001g0103 a0001c0001t0001g0196 |
3 | HG02818.hp1 HG03486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.770-2280A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561566 | |||||||
chr19:29561715 | C | A | 3 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0002c0002t0001g0307 |
4 | NA18948.hp1 NA18977.hp1 NA18988.hp1 others(1): Show |
intron_variant | MODIFIER | c.770-2131C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561715 | |||||||
chr19:29561750 | C | A | 3 | a0001c0001t0001g0112 a0001c0001t0001g0115 a0001c0001t0002g0116 |
3 | HG02602.hp1 HG02683.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.770-2096C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561750 | |||||||
chr19:29561753 | G | A | 1 | a0002c0002t0001g0292 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.770-2093G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561753 | |||||||
chr19:29561756 | C | A | 23 | a0001c0001t0001g0014 a0001c0001t0001g0036 a0001c0001t0001g0068 others(20): Show |
27 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(24): Show |
intron_variant | MODIFIER | c.770-2090C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561756 | |||||||
chr19:29561842 | C | A | 1 | a0001c0004t0001g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.770-2004C>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561842 | |||||||
chr19:29561859 | T | C | 11 | a0001c0001t0001g0034 a0001c0001t0001g0237 a0001c0001t0001g0238 others(8): Show |
13 | HG02135.hp1 NA18948.hp1 NA18952.hp1 others(10): Show |
intron_variant | MODIFIER | c.770-1987T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561859 | |||||||
chr19:29561921 | G | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0153 a0001c0001t0001g0154 others(11): Show |
15 | HG00639.hp2 HG01891.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.770-1925G>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29561921 | |||||||
chr19:29562035 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.770-1811C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562035 | |||||||
chr19:29562291 | C | T | 5 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0121 others(2): Show |
7 | HG00735.hp1 HG01346.hp1 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.770-1555C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562291 | |||||||
chr19:29562375 | C | G | 1 | a0001c0001t0001g0219 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.770-1471C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562375 | |||||||
chr19:29562460 | G | A | 2 | a0001c0004t0001g0191 a0001c0004t0001g0192 |
2 | HG01109.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.770-1386G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562460 | |||||||
chr19:29562502 | G | A | 1 | a0003c0006t0001g0343 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.770-1344G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562502 | |||||||
chr19:29562504 | C | T | 1 | a0002c0002t0001g0336 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.770-1342C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562504 | |||||||
chr19:29562558 | G | C | 3 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0003g0085 |
3 | HG03130.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.770-1288G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562558 | |||||||
chr19:29562609 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.770-1237C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562609 | |||||||
chr19:29562638 | G | A | 5 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0003t0003g0058 others(2): Show |
5 | HG02280.hp2 HG02965.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.770-1208G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562638 | |||||||
chr19:29562665 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0072 a0001c0001t0001g0102 others(1): Show |
5 | HG01884.hp2 HG02809.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.770-1181G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562665 | |||||||
chr19:29562669 | G | C | 1 | a0001c0001t0001g0164 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.770-1177G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562669 | |||||||
chr19:29562822 | A | G | 44 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0023 others(41): Show |
49 | HG00408.hp1 HG00609.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.770-1024A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562822 | |||||||
chr19:29562891 | A | C | 80 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0027 others(77): Show |
87 | HG00408.hp2 HG00438.hp1 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.770-955A>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562891 | |||||||
chr19:29562894 | C | T | 129 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0024 others(126): Show |
144 | HG00408.hp2 HG00438.hp1 HG00544.hp2 others(141): Show |
intron_variant | MODIFIER | c.770-952C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29562894 | |||||||
chr19:29563069 | C | G | 23 | a0001c0001t0001g0092 a0001c0001t0001g0096 a0001c0001t0001g0127 others(20): Show |
30 | HG00544.hp2 HG00558.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.770-777C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563069 | |||||||
chr19:29563160 | G | C | 103 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(100): Show |
118 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.770-686G>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563160 | |||||||
chr19:29563248 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.770-598G>A | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563248 | |||||||
chr19:29563250 | C | CT | 226 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(223): Show |
257 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.770-584dupT | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29563250 | ||||||
chr19:29563283 | C | T | 14 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0227 others(11): Show |
17 | HG00544.hp1 HG02056.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-563C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563283 | |||||||
chr19:29563313 | T | TGCA | 14 | a0001c0001t0002g0169 a0001c0001t0002g0174 a0001c0001t0002g0227 others(11): Show |
17 | HG00544.hp1 HG02056.hp2 HG02132.hp2 others(14): Show |
intron_variant | MODIFIER | c.770-532_770-530dup others(3): Show |
VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr19 | 29563313 | ||||||
chr19:29563341 | C | T | 1 | a0001c0001t0001g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.770-505C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563341 | |||||||
chr19:29563404 | C | T | 1 | a0001c0001t0001g0226 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.770-442C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563404 | |||||||
chr19:29563468 | C | G | 3 | a0001c0001t0001g0131 a0001c0004t0001g0066 a0006c0009t0001g0283 |
3 | HG01361.hp2 HG02145.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.770-378C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563468 | |||||||
chr19:29563633 | T | C | 1 | a0001c0001t0001g0208 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.770-213T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563633 | |||||||
chr19:29563648 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.770-198T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563648 | |||||||
chr19:29563687 | A | G | 1 | a0002c0002t0001g0250 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.770-159A>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563687 | |||||||
chr19:29563710 | T | C | 15 | a0001c0001t0002g0116 a0001c0001t0002g0169 a0001c0001t0002g0174 others(12): Show |
18 | HG00544.hp1 HG02056.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.770-136T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563710 | |||||||
chr19:29563822 | T | C | 2 | a0001c0001t0001g0152 a0001c0003t0001g0055 |
2 | HG01081.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.770-24T>C | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563822 | |||||||
chr19:29563838 | C | T | 6 | a0001c0001t0003g0085 a0001c0001t0003g0106 a0001c0001t0003g0268 others(3): Show |
6 | HG02717.hp1 HG03130.hp1 HG03195.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.770-8C>T | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563838 | |||||||
chr19:29563839 | C | G | 15 | a0001c0001t0002g0116 a0001c0001t0002g0169 a0001c0001t0002g0174 others(12): Show |
18 | HG00544.hp1 HG02056.hp2 HG02132.hp2 others(15): Show |
splice_region_variant&intron_variant | LOW | c.770-7C>G | VSTM2B | ENSG00000187135.8 | transcript | ENST00000335523.8 | protein_coding | 4/4 | chr19 | 29563839 |