Item | Value |
---|---|
geneid | 29888 |
ensemblid | ENSG00000090372.15 |
hgncid | 15721 |
symbol | STRN4 |
name | striatin 4 |
refseq_nuc | NM_013403.3 |
refseq_prot | NP_037535.2 |
ensembl_nuc | ENST00000263280.11 |
ensembl_prot | ENSP00000263280.4 |
mane_status | MANE Select |
chr | chr19 |
start | 46719511 |
end | 46746450 |
strand | - |
ver | v1.2 |
region | chr19:46719511-46746450 |
region5000 | chr19:46714511-46751450 |
regionname0 | STRN4_chr19_46719511_46746450 |
regionname5000 | STRN4_chr19_46714511_46751450 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 753 | 367 | 74 | 73 | 161 | 14 | 43 | 123 | STRN4_chr19_46714511_46751450 | STRN4 | MMEER others(748): Show |
chr19 | 46714511 | 46751450 |
a0002 | 0/0 | 753 | 31 | 20 | 5 | 5 | 0 | 1 | 4 | STRN4_chr19_46714511_46751450 | STRN4 | MMEER others(748): Show |
chr19 | 46714511 | 46751450 |
a0003 | 0/0 | 753 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | MMEER others(748): Show |
chr19 | 46714511 | 46751450 |
a0004 | 0/0 | 753 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | MMEER others(748): Show |
chr19 | 46714511 | 46751450 |
a0005 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | MMEER others(748): Show |
chr19 | 46714511 | 46751450 |
a0006 | 0/0 | 753 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | MMEER others(748): Show |
chr19 | 46714511 | 46751450 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2259 | 295 | 51 | 61 | 134 | 12 | 35 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0002 | 0/0 | 2259 | 37 | 11 | 7 | 11 | 2 | 6 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0004 | 0/0 | 2259 | 19 | 0 | 3 | 14 | 0 | 2 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0005 | 0/0 | 2259 | 7 | 7 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0006 | 0/0 | 2259 | 5 | 4 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0007 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0008 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0010 | 0/0 | 2259 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0001c0011 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0002c0003 | 0/0 | 2259 | 31 | 20 | 5 | 5 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0003c0014 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0004c0013 | 0/0 | 2259 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0005c0009 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 | ||
a0006c0012 | 0/0 | 2259 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | ATGAT others(2254): Show |
chr19 | 46714511 | 46751450 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3176 | 170 | 38 | 35 | 61 | 10 | 25 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0002 | 1/0 | 3176 | 79 | 8 | 16 | 47 | 1 | 6 | STRN4_chr19_46714511_46751450 | STRN4 | AGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0003 | 0/0 | 3176 | 38 | 5 | 6 | 22 | 1 | 4 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0005 | 0/0 | 3176 | 2 | 0 | 2 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0007 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | AGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0008 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | AGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0009 | 0/0 | 3176 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0010 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0011 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0001t0012 | 0/0 | 3176 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0002t0001 | 0/0 | 3176 | 20 | 8 | 6 | 0 | 2 | 4 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0002t0004 | 0/0 | 3176 | 17 | 3 | 1 | 11 | 0 | 2 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0004t0001 | 0/0 | 3176 | 18 | 0 | 3 | 13 | 0 | 2 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0004t0003 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0005t0001 | 0/0 | 3176 | 7 | 7 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0006t0001 | 0/0 | 3176 | 5 | 4 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0007t0001 | 0/0 | 3176 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0008t0002 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | AGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0010t0001 | 0/0 | 3176 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0001c0011t0001 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0002c0003t0001 | 0/0 | 3176 | 29 | 20 | 5 | 3 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0002c0003t0006 | 0/0 | 3176 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0003c0014t0003 | 0/0 | 3176 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0004c0013t0001 | 0/0 | 3176 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0005c0009t0001 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
a0006c0012t0003 | 0/0 | 3176 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | GGGCC others(3171): Show |
chr19 | 46714511 | 46751450 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 16 | 0 | 6 | 7 | 1 | 2 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0003 | 0/0 | 11 | 1 | 3 | 6 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0004 | 0/0 | 10 | 1 | 3 | 0 | 4 | 2 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0006 | 0/0 | 7 | 0 | 4 | 1 | 0 | 2 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0007 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0009 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0012 | 0/0 | 5 | 0 | 4 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0041 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0042 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0048 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0194 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0001 | 0/0 | 24 | 0 | 10 | 10 | 1 | 3 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0015 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0033 | 1/0 | 2 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0016 | 0/0 | 4 | 0 | 2 | 1 | 1 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0022 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0025 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0049 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0005g0038 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0007g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0009g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0010g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0011g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0001t0012g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0005 | 0/0 | 8 | 6 | 2 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0008 | 0/0 | 5 | 0 | 3 | 0 | 2 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0002t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0013 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0004t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0005t0001g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0005t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0005t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0005t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0005t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0006t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0006t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0006t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0006t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0006t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0007t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0008t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0010t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0001c0011t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0024 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0047 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0006g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0002c0003t0006g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0003c0014t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0004c0013t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0005c0009t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
a0006c0012t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | GBR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00280 | hp1 | a0001 | c0002 | t0001 | g0008 | EUR | FIN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | FIN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00323 | hp2 | a0001 | c0002 | t0001 | g0008 | EUR | FIN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00423 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00544 | hp2 | a0001 | c0004 | t0001 | g0249 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00609 | hp2 | a0001 | c0004 | t0001 | g0026 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00621 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00639 | hp2 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00733 | hp1 | a0002 | c0003 | t0001 | g0201 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00735 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00738 | hp1 | a0002 | c0003 | t0001 | g0207 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0245 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01070 | hp1 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01070 | hp2 | a0001 | c0007 | t0001 | g0139 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01071 | hp2 | a0001 | c0001 | t0005 | g0038 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01074 | hp2 | a0002 | c0003 | t0001 | g0200 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0184 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01175 | hp1 | a0001 | c0002 | t0001 | g0008 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0113 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01243 | hp2 | a0002 | c0003 | t0001 | g0208 | AMR | PUR | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01261 | hp1 | a0001 | c0006 | t0001 | g0074 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01358 | hp2 | a0001 | c0002 | t0001 | g0060 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01361 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0111 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01433 | hp2 | a0001 | c0001 | t0012 | g0131 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01496 | hp2 | a0001 | c0002 | t0001 | g0005 | AMR | CLM | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0016 | EUR | IBS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0142 | EUR | IBS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0004 | EUR | IBS | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01884 | hp1 | a0002 | c0003 | t0001 | g0047 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01934 | hp1 | a0003 | c0014 | t0003 | g0250 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01934 | hp2 | a0002 | c0003 | t0001 | g0215 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0016 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01943 | hp2 | a0001 | c0002 | t0004 | g0117 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01975 | hp1 | a0001 | c0001 | t0009 | g0177 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG01993 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02004 | hp2 | a0004 | c0013 | t0001 | g0220 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0100 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0180 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02055 | hp2 | a0002 | c0003 | t0001 | g0214 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02080 | hp1 | a0001 | c0008 | t0002 | g0128 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02083 | hp1 | a0002 | c0003 | t0001 | g0236 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02129 | hp2 | a0005 | c0009 | t0001 | g0120 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02135 | hp2 | a0001 | c0004 | t0001 | g0026 | EAS | KHV | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02145 | hp1 | a0001 | c0006 | t0001 | g0235 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0044 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | CDX | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | CDX | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02165 | hp1 | a0001 | c0004 | t0001 | g0241 | EAS | CDX | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | CDX | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02257 | hp2 | a0002 | c0003 | t0001 | g0237 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0054 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02280 | hp2 | a0001 | c0005 | t0001 | g0051 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02293 | hp2 | a0001 | c0004 | t0001 | g0013 | AMR | PEL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0183 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02572 | hp2 | a0001 | c0005 | t0001 | g0018 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02602 | hp2 | a0001 | c0002 | t0001 | g0056 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0086 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0211 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02630 | hp1 | a0001 | c0005 | t0001 | g0053 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02630 | hp2 | a0001 | c0002 | t0004 | g0019 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02647 | hp2 | a0002 | c0003 | t0001 | g0209 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0033 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02717 | hp1 | a0002 | c0003 | t0001 | g0123 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02717 | hp2 | a0001 | c0005 | t0001 | g0018 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0146 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0052 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02886 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02896 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02897 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02922 | hp1 | a0001 | c0002 | t0004 | g0019 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02965 | hp1 | a0001 | c0006 | t0001 | g0065 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0050 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02976 | hp2 | a0001 | c0005 | t0001 | g0018 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03041 | hp2 | a0002 | c0003 | t0001 | g0212 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03209 | hp2 | a0001 | c0002 | t0004 | g0019 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0015 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0191 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03490 | hp2 | a0001 | c0002 | t0004 | g0114 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03516 | hp1 | a0002 | c0003 | t0001 | g0124 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | ESN | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03540 | hp1 | a0001 | c0002 | t0001 | g0005 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0041 | AFR | GWD | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03579 | hp2 | a0001 | c0006 | t0001 | g0073 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03688 | hp1 | a0001 | c0004 | t0001 | g0246 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0185 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03710 | hp2 | a0001 | c0002 | t0001 | g0058 | SAS | PJL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0061 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03942 | hp1 | a0001 | c0002 | t0001 | g0057 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0216 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0231 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0049 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0233 | SAS | BEB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04199 | hp1 | a0001 | c0002 | t0004 | g0116 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04204 | hp1 | a0001 | c0001 | t0003 | g0136 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0187 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04228 | hp1 | a0001 | c0004 | t0001 | g0248 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG04228 | hp2 | a0002 | c0003 | t0001 | g0230 | SAS | STU | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0085 | AFR | YRI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18522 | hp2 | a0001 | c0010 | t0001 | g0203 | AFR | YRI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0070 | EAS | CHB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18747 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | CHB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | CHB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18906 | hp1 | a0002 | c0003 | t0001 | g0024 | AFR | YRI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18942 | hp1 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18947 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0089 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18951 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18953 | hp1 | a0001 | c0001 | t0003 | g0049 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18961 | hp1 | a0001 | c0004 | t0001 | g0247 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18963 | hp1 | a0002 | c0003 | t0001 | g0205 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18964 | hp1 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18965 | hp2 | a0001 | c0011 | t0001 | g0228 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18967 | hp2 | a0001 | c0002 | t0004 | g0127 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18973 | hp2 | a0001 | c0004 | t0001 | g0240 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18978 | hp1 | a0001 | c0001 | t0007 | g0105 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18979 | hp2 | a0006 | c0012 | t0003 | g0229 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18980 | hp2 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18982 | hp1 | a0001 | c0004 | t0001 | g0239 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18984 | hp1 | a0001 | c0004 | t0003 | g0243 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18984 | hp2 | a0001 | c0001 | t0011 | g0144 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18985 | hp2 | a0002 | c0003 | t0006 | g0063 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18986 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18991 | hp1 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18991 | hp2 | a0001 | c0001 | t0010 | g0110 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18993 | hp1 | a0001 | c0004 | t0001 | g0244 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0109 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18999 | hp1 | a0002 | c0003 | t0001 | g0206 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19009 | hp1 | a0001 | c0004 | t0001 | g0026 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0242 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0094 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19030 | hp1 | a0002 | c0003 | t0001 | g0210 | AFR | LWK | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19030 | hp2 | a0002 | c0003 | t0001 | g0024 | AFR | LWK | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19043 | hp1 | a0002 | c0003 | t0001 | g0199 | AFR | LWK | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | LWK | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19057 | hp2 | a0001 | c0002 | t0004 | g0115 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19063 | hp1 | a0001 | c0002 | t0004 | g0118 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19065 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19065 | hp2 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19066 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19067 | hp1 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19067 | hp2 | a0002 | c0003 | t0006 | g0062 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19068 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19077 | hp1 | a0001 | c0004 | t0001 | g0013 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0068 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0021 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19088 | hp2 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19089 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19091 | hp2 | a0001 | c0001 | t0003 | g0126 | EAS | JPT | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0028 | AFR | YRI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA19240 | hp2 | a0002 | c0003 | t0001 | g0023 | AFR | YRI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ASW | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ASW | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | GIH | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02109 | hp2 | a0002 | c0003 | t0001 | g0047 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02486 | hp2 | a0002 | c0003 | t0001 | g0125 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02559 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03471 | hp1 | a0002 | c0003 | t0001 | g0202 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0005 | AFR | MSL | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | USA | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | USA | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20300 | hp1 | a0001 | c0006 | t0001 | g0067 | AFR | USA | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA21309 | hp1 | a0002 | c0003 | t0001 | g0213 | AFR | LWK | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | LWK | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0194 | REF | REF | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0033 | REF | REF | STRN4_chr19_46714511_46751450 | STRN4 | chr19 | 46714511 | 46751450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46723177 | C | T | 1 | a0002 | 31 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(28): Show |
missense_variant | MODERATE | c.1702G>A | p.Val568Ile | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 13/18 | 1722/3176 | 1702/2262 | 568/753 | chr19 | 46723177 | |||
chr19:46724899 | C | A | 1 | a0006 | 1 | NA18979.hp2 | missense_variant | MODERATE | c.1502G>T | p.Ser501Ile | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/18 | 1522/3176 | 1502/2262 | 501/753 | chr19 | 46724899 | |||
chr19:46727974 | G | T | 1 | a0005 | 1 | HG02129.hp2 | missense_variant | MODERATE | c.1073C>A | p.Ala358Asp | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 8/18 | 1093/3176 | 1073/2262 | 358/753 | chr19 | 46727974 | |||
chr19:46733184 | G | A | 1 | a0004 | 1 | HG02004.hp2 | missense_variant | MODERATE | c.592C>T | p.Arg198Cys | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/18 | 612/3176 | 592/2262 | 198/753 | chr19 | 46733184 | |||
chr19:46746360 | G | C | 1 | a0003 | 1 | HG01934.hp1 | missense_variant | MODERATE | c.71C>G | p.Ala24Gly | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/18 | 91/3176 | 71/2262 | 24/753 | chr19 | 46746360 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46720692 | G | A | 1 | a0001c0002 | 37 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(34): Show |
synonymous_variant | LOW | c.2172C>T | p.His724His | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 17/18 | 2192/3176 | 2172/2262 | 724/753 | chr19 | 46720692 | |||
chr19:46722008 | G | A | 2 | a0001c0004 a0001c0011 |
20 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(17): Show |
synonymous_variant | LOW | c.2070C>T | p.Asn690Asn | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/18 | 2090/3176 | 2070/2262 | 690/753 | chr19 | 46722008 | |||
chr19:46723193 | A | G | 2 | a0001c0010 a0002c0003 |
32 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(29): Show |
synonymous_variant | LOW | c.1686T>C | p.Cys562Cys | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 13/18 | 1706/3176 | 1686/2262 | 562/753 | chr19 | 46723193 | |||
chr19:46730873 | C | T | 1 | a0001c0008 | 1 | HG02080.hp1 | splice_region_variant&synonymous_variant | LOW | c.738G>A | p.Arg246Arg | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/18 | 758/3176 | 738/2262 | 246/753 | chr19 | 46730873 | |||
chr19:46736888 | G | A | 1 | a0001c0006 | 5 | HG01261.hp1 HG02145.hp1 HG02965.hp1 others(2): Show |
synonymous_variant | LOW | c.474C>T | p.Pro158Pro | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/18 | 494/3176 | 474/2262 | 158/753 | chr19 | 46736888 | |||
chr19:46738799 | C | T | 1 | a0001c0007 | 1 | HG01070.hp2 | synonymous_variant | LOW | c.372G>A | p.Ala124Ala | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/18 | 392/3176 | 372/2262 | 124/753 | chr19 | 46738799 | |||
chr19:46746347 | G | C | 1 | a0001c0004 | 19 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(16): Show |
synonymous_variant | LOW | c.84C>G | p.Pro28Pro | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/18 | 104/3176 | 84/2262 | 28/753 | chr19 | 46746347 | |||
chr19:46746401 | G | T | 1 | a0001c0005 | 7 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(4): Show |
synonymous_variant | LOW | c.30C>A | p.Val10Val | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/18 | 50/3176 | 30/2262 | 10/753 | chr19 | 46746401 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46719544 | C | T | 1 | a0001c0001t0011 | 1 | NA18984.hp2 | 3_prime_UTR_variant | MODIFIER | c.*861G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 1058 | chr19 | 46719544 | ||||||
chr19:46719667 | A | G | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 935 | chr19 | 46719667 | ||||||
chr19:46719668 | G | A | 1 | a0001c0001t0007 | 1 | NA18978.hp1 | 3_prime_UTR_variant | MODIFIER | c.*737C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 934 | chr19 | 46719668 | ||||||
chr19:46719709 | G | A | 1 | a0001c0001t0012 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 893 | chr19 | 46719709 | ||||||
chr19:46719907 | G | A | 1 | a0001c0001t0012 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*498C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 695 | chr19 | 46719907 | ||||||
chr19:46719926 | G | A | 1 | a0002c0003t0006 | 2 | NA18985.hp2 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*479C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 676 | chr19 | 46719926 | ||||||
chr19:46720037 | C | T | 5 | a0001c0001t0003 a0001c0001t0009 a0001c0004t0003 others(2): Show |
42 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*368G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 565 | chr19 | 46720037 | ||||||
chr19:46720083 | C | T | 1 | a0001c0001t0005 | 2 | HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*322G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 519 | chr19 | 46720083 | ||||||
chr19:46720142 | G | A | 1 | a0001c0002t0004 | 17 | HG00423.hp2 HG00621.hp1 HG01943.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*263C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 460 | chr19 | 46720142 | ||||||
chr19:46720286 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*119A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 316 | chr19 | 46720286 | ||||||
chr19:46720289 | C | T | 1 | a0001c0001t0009 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*116G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 18/18 | 313 | chr19 | 46720289 | ||||||
chr19:46746450 | T | C | 22 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(19): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
5_prime_UTR_variant | MODIFIER | c.-20A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/18 | 20 | chr19 | 46746450 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:46720371 | C | T | 4 | a0001c0001t0001g0012 a0001c0001t0001g0195 a0001c0001t0001g0198 others(1): Show |
8 | HG01081.hp2 HG01099.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.*67-33G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 17/17 | chr19 | 46720371 | |||||||
chr19:46720776 | A | G | 1 | a0001c0001t0002g0097 | 1 | HG02080.hp2 | splice_region_variant&intron_variant | LOW | c.2093-5T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46720776 | |||||||
chr19:46720816 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2093-45C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46720816 | |||||||
chr19:46720923 | G | A | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2093-152C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46720923 | |||||||
chr19:46721060 | C | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
intron_variant | MODIFIER | c.2093-289G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721060 | |||||||
chr19:46721174 | C | T | 2 | a0001c0001t0001g0045 a0001c0001t0003g0178 |
3 | HG02258.hp1 HG02723.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.2093-403G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721174 | |||||||
chr19:46721175 | G | A | 2 | a0001c0001t0001g0166 a0001c0001t0001g0169 |
2 | NA18964.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2093-404C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721175 | |||||||
chr19:46721186 | TGAGGCAG others(3): Show |
T | 1 | a0001c0001t0002g0028 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2093-425_2093-416d others(12): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721186 | |||||||
chr19:46721223 | A | G | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2093-452T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721223 | |||||||
chr19:46721227 | A | G | 200 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(197): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.2093-456T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721227 | |||||||
chr19:46721280 | G | T | 1 | a0001c0001t0003g0176 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.2093-509C>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721280 | |||||||
chr19:46721333 | C | T | 33 | a0001c0001t0001g0135 a0001c0001t0001g0150 a0001c0001t0001g0217 others(30): Show |
44 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.2093-562G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721333 | |||||||
chr19:46721350 | C | T | 108 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(105): Show |
179 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.2093-579G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721350 | |||||||
chr19:46721389 | T | C | 9 | a0001c0002t0004g0010 a0001c0002t0004g0037 a0001c0002t0004g0068 others(6): Show |
14 | HG00423.hp2 HG00621.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.2092+597A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721389 | |||||||
chr19:46721443 | A | G | 3 | a0002c0003t0001g0212 a0002c0003t0001g0215 a0002c0003t0001g0237 |
3 | HG01934.hp2 HG02257.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.2092+543T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721443 | |||||||
chr19:46721574 | T | C | 1 | a0001c0001t0010g0110 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2092+412A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721574 | |||||||
chr19:46721614 | T | C | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2092+372A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721614 | |||||||
chr19:46721661 | C | G | 27 | a0001c0010t0001g0203 a0002c0003t0001g0023 a0002c0003t0001g0024 others(24): Show |
32 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.2092+325G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721661 | |||||||
chr19:46721730 | A | C | 1 | a0001c0006t0001g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2092+256T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721730 | |||||||
chr19:46721775 | A | G | 1 | a0002c0003t0001g0211 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2092+211T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721775 | |||||||
chr19:46721791 | G | A | 1 | a0001c0001t0002g0095 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2092+195C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721791 | |||||||
chr19:46721844 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.2092+142A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721844 | |||||||
chr19:46721864 | G | A | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2092+122C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 16/17 | chr19 | 46721864 | |||||||
chr19:46722120 | C | T | 3 | a0001c0001t0001g0147 a0001c0001t0001g0158 a0001c0001t0001g0222 |
3 | HG00140.hp1 HG01192.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.2006-48G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 15/17 | chr19 | 46722120 | |||||||
chr19:46722131 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2006-59C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 15/17 | chr19 | 46722131 | |||||||
chr19:46722146 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2006-74C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 15/17 | chr19 | 46722146 | |||||||
chr19:46722346 | G | A | 1 | a0002c0003t0001g0207 | 1 | HG00738.hp1 | splice_region_variant&intron_variant | LOW | c.1907-6C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722346 | |||||||
chr19:46722416 | C | T | 12 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0199 others(9): Show |
16 | HG00733.hp1 HG01074.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1907-76G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722416 | |||||||
chr19:46722440 | T | C | 1 | a0001c0001t0003g0181 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1907-100A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722440 | |||||||
chr19:46722441 | G | T | 1 | a0001c0001t0003g0181 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1907-101C>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722441 | |||||||
chr19:46722442 | C | G | 1 | a0001c0001t0003g0181 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.1907-102G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722442 | |||||||
chr19:46722460 | C | T | 1 | a0001c0001t0002g0094 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1907-120G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722460 | |||||||
chr19:46722492 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1907-152G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722492 | |||||||
chr19:46722496 | G | A | 27 | a0001c0010t0001g0203 a0002c0003t0001g0023 a0002c0003t0001g0024 others(24): Show |
32 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1907-156C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722496 | |||||||
chr19:46722533 | C | CT | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(173): Show |
271 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.1907-194_1907-193i others(3): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722533 | |||||||
chr19:46722534 | G | A | 1 | a0001c0001t0002g0096 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1907-194C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722534 | |||||||
chr19:46722546 | A | G | 40 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0020 others(37): Show |
59 | HG00438.hp1 HG00544.hp2 HG00597.hp1 others(56): Show |
intron_variant | MODIFIER | c.1907-206T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722546 | |||||||
chr19:46722554 | C | G | 1 | a0002c0003t0001g0200 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1907-214G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722554 | |||||||
chr19:46722592 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1906+218C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722592 | |||||||
chr19:46722609 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1906+201G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722609 | |||||||
chr19:46722754 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1906+56T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722754 | |||||||
chr19:46722768 | G | A | 2 | a0002c0003t0006g0062 a0002c0003t0006g0063 |
2 | NA18985.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.1906+42C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 14/17 | chr19 | 46722768 | |||||||
chr19:46723562 | GCTCAATA others(4): Show |
G | 1 | a0001c0001t0002g0078 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1595-289_1595-279d others(13): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723562 | |||||||
chr19:46723620 | C | T | 1 | a0001c0001t0003g0175 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1595-336G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723620 | |||||||
chr19:46723673 | C | A | 1 | a0001c0001t0007g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1595-389G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723673 | |||||||
chr19:46723739 | T | C | 1 | a0001c0001t0007g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1595-455A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723739 | |||||||
chr19:46723793 | T | TCTGGCCT others(13): Show |
1 | a0001c0002t0001g0056 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1595-529_1595-510d others(22): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723793 | |||||||
chr19:46723797 | G | C | 1 | a0001c0001t0007g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1595-513C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723797 | |||||||
chr19:46723798 | C | G | 1 | a0001c0001t0007g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1595-514G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723798 | |||||||
chr19:46723818 | G | A | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1595-534C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46723818 | |||||||
chr19:46724038 | C | A | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
229 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(226): Show |
intron_variant | MODIFIER | c.1595-754G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724038 | |||||||
chr19:46724063 | C | T | 1 | a0001c0004t0001g0240 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1594+744G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724063 | |||||||
chr19:46724070 | C | A | 154 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(151): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.1594+737G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724070 | |||||||
chr19:46724112 | G | A | 1 | a0001c0004t0003g0243 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1594+695C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724112 | |||||||
chr19:46724119 | G | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1594+688C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724119 | |||||||
chr19:46724164 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1594+643G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724164 | |||||||
chr19:46724243 | T | G | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1594+564A>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724243 | |||||||
chr19:46724245 | G | C | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1594+562C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724245 | |||||||
chr19:46724248 | T | A | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1594+559A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724248 | |||||||
chr19:46724249 | C | A | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1594+558G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CA | 12 | a0001c0001t0002g0015 a0001c0001t0002g0030 a0001c0001t0002g0036 others(9): Show |
17 | HG00423.hp1 HG00621.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.1594+557dupT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAA | 10 | a0001c0001t0001g0046 a0001c0001t0002g0029 a0001c0001t0002g0031 others(7): Show |
13 | HG00642.hp1 HG00733.hp1 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.1594+556_1594+557d others(4): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAA | 6 | a0001c0001t0001g0077 a0001c0001t0002g0091 a0001c0004t0001g0013 others(3): Show |
10 | HG01993.hp2 HG02293.hp2 HG03688.hp1 others(7): Show |
intron_variant | MODIFIER | c.1594+554_1594+557d others(6): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAA | 6 | a0001c0004t0001g0026 a0001c0004t0001g0240 a0001c0004t0001g0241 others(3): Show |
8 | HG00609.hp2 HG02135.hp2 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.1594+553_1594+557d others(7): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(3): Show |
16 | a0001c0001t0001g0041 a0001c0001t0001g0217 a0001c0001t0002g0078 others(13): Show |
21 | HG00609.hp1 HG01106.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1594+548_1594+557d others(12): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(4): Show |
18 | a0001c0001t0001g0020 a0001c0001t0001g0080 a0001c0001t0001g0083 others(15): Show |
29 | HG01081.hp1 HG01346.hp1 HG01515.hp2 others(26): Show |
intron_variant | MODIFIER | c.1594+547_1594+557d others(13): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(5): Show |
13 | a0001c0001t0001g0007 a0001c0001t0001g0034 a0001c0001t0001g0072 others(10): Show |
18 | HG00597.hp1 HG00597.hp2 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.1594+546_1594+557d others(14): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(6): Show |
6 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0082 others(3): Show |
7 | HG00673.hp1 HG02129.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+545_1594+557d others(15): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(7): Show |
3 | a0001c0001t0001g0055 a0001c0001t0002g0086 a0002c0003t0001g0199 |
3 | HG01261.hp2 HG02615.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1594+544_1594+557d others(16): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(8): Show |
2 | a0001c0001t0002g0028 a0002c0003t0006g0062 |
3 | HG02809.hp2 NA19067.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1594+543_1594+557d others(17): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(10): Show |
1 | a0002c0003t0006g0063 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1594+541_1594+557d others(19): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(13): Show |
1 | a0002c0003t0001g0202 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1594+538_1594+557d others(22): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | C | CAAAAAAA others(15): Show |
1 | a0001c0006t0001g0073 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1594+536_1594+557d others(24): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | CA | C | 17 | a0001c0001t0001g0009 a0001c0001t0001g0066 a0001c0001t0001g0088 others(14): Show |
22 | HG00438.hp1 HG01167.hp2 HG01243.hp2 others(19): Show |
intron_variant | MODIFIER | c.1594+557delT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | CAAAAA | C | 65 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(62): Show |
119 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1594+553_1594+557d others(7): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1594+548_1594+557d others(12): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | CAAAAAAA others(4): Show |
C | 10 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(7): Show |
23 | HG00280.hp2 HG00639.hp1 HG01081.hp2 others(20): Show |
intron_variant | MODIFIER | c.1594+547_1594+557d others(13): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724249 | CAAAAAAA others(13): Show |
C | 3 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0200 |
7 | HG01074.hp2 HG02886.hp2 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1594+538_1594+557d others(22): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724249 | |||||||
chr19:46724370 | G | A | 12 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0199 others(9): Show |
16 | HG00733.hp1 HG01074.hp2 HG02083.hp1 others(13): Show |
intron_variant | MODIFIER | c.1594+437C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724370 | |||||||
chr19:46724449 | C | T | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1594+358G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724449 | |||||||
chr19:46724450 | G | C | 4 | a0002c0003t0001g0208 a0002c0003t0001g0209 a0002c0003t0001g0213 others(1): Show |
4 | HG01243.hp2 HG02055.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.1594+357C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724450 | |||||||
chr19:46724470 | C | T | 10 | a0002c0003t0001g0047 a0002c0003t0001g0208 a0002c0003t0001g0209 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.1594+337G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724470 | |||||||
chr19:46724472 | C | A | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1594+335G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724472 | |||||||
chr19:46724508 | G | A | 15 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0004t0001g0013 others(12): Show |
21 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.1594+299C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724508 | |||||||
chr19:46724563 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1594+244G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724563 | |||||||
chr19:46724564 | G | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0045 others(25): Show |
48 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(45): Show |
intron_variant | MODIFIER | c.1594+243C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724564 | |||||||
chr19:46724586 | G | C | 13 | a0001c0004t0001g0013 a0001c0004t0001g0026 a0001c0004t0001g0239 others(10): Show |
19 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1594+221C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724586 | |||||||
chr19:46724751 | A | T | 1 | a0001c0001t0001g0156 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1594+56T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724751 | |||||||
chr19:46724780 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1594+27C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 12/17 | chr19 | 46724780 | |||||||
chr19:46725108 | A | G | 13 | a0001c0004t0001g0013 a0001c0004t0001g0026 a0001c0004t0001g0239 others(10): Show |
19 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1473-180T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 11/17 | chr19 | 46725108 | |||||||
chr19:46725209 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1472+123C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 11/17 | chr19 | 46725209 | |||||||
chr19:46725264 | A | T | 13 | a0001c0004t0001g0013 a0001c0004t0001g0026 a0001c0004t0001g0239 others(10): Show |
19 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.1472+68T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 11/17 | chr19 | 46725264 | |||||||
chr19:46725450 | G | A | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1424+23C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 10/17 | chr19 | 46725450 | |||||||
chr19:46725728 | G | C | 248 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
398 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(395): Show |
intron_variant | MODIFIER | c.1249-80C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46725728 | |||||||
chr19:46725733 | T | C | 124 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(121): Show |
193 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(190): Show |
intron_variant | MODIFIER | c.1249-85A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46725733 | |||||||
chr19:46725733 | T | G | 1 | a0001c0001t0003g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1249-85A>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46725733 | |||||||
chr19:46725783 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1249-135G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46725783 | |||||||
chr19:46725956 | T | C | 1 | a0001c0001t0002g0102 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1249-308A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46725956 | |||||||
chr19:46726040 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1249-392G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726040 | |||||||
chr19:46726107 | G | A | 1 | a0001c0006t0001g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1249-459C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726107 | |||||||
chr19:46726225 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1249-577C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726225 | |||||||
chr19:46726254 | A | T | 1 | a0001c0001t0001g0137 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1249-606T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726254 | |||||||
chr19:46726326 | G | A | 2 | a0001c0001t0002g0098 a0001c0001t0002g0099 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1249-678C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726326 | |||||||
chr19:46726383 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1249-735C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726383 | |||||||
chr19:46726483 | C | CA | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
158 | HG00140.hp1 HG00544.hp1 HG00558.hp2 others(155): Show |
intron_variant | MODIFIER | c.1249-836dupT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726483 | |||||||
chr19:46726483 | CA | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0009 others(103): Show |
161 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(158): Show |
intron_variant | MODIFIER | c.1249-836delT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726483 | |||||||
chr19:46726657 | C | G | 1 | a0001c0002t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1248+795G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726657 | |||||||
chr19:46726697 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0190 |
2 | HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1248+755G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726697 | |||||||
chr19:46726768 | T | C | 14 | a0002c0003t0001g0047 a0002c0003t0001g0123 a0002c0003t0001g0124 others(11): Show |
15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.1248+684A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726768 | |||||||
chr19:46726824 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1248+628G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726824 | |||||||
chr19:46726856 | C | T | 152 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(149): Show |
235 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(232): Show |
intron_variant | MODIFIER | c.1248+596G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726856 | |||||||
chr19:46726903 | A | T | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1248+549T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46726903 | |||||||
chr19:46727044 | AGCTCCCA others(11): Show |
A | 3 | a0002c0003t0001g0208 a0002c0003t0001g0213 a0002c0003t0001g0214 |
3 | HG01243.hp2 HG02055.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1248+390_1248+407d others(20): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46727044 | |||||||
chr19:46727056 | G | A | 1 | a0001c0001t0002g0104 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1248+396C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46727056 | |||||||
chr19:46727084 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG00738.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1248+368G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46727084 | |||||||
chr19:46727136 | C | CT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0045 others(24): Show |
47 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.1248+315_1248+316i others(3): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46727136 | |||||||
chr19:46727304 | C | A | 3 | a0001c0001t0001g0027 a0001c0001t0001g0081 a0001c0001t0001g0112 |
4 | HG00673.hp1 HG02129.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.1248+148G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46727304 | |||||||
chr19:46727370 | C | T | 13 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0048 others(10): Show |
21 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.1248+82G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 9/17 | chr19 | 46727370 | |||||||
chr19:46727583 | G | T | 1 | a0001c0001t0003g0184 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1154-37C>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 8/17 | chr19 | 46727583 | |||||||
chr19:46727627 | G | C | 1 | a0001c0001t0002g0102 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1154-81C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 8/17 | chr19 | 46727627 | |||||||
chr19:46727663 | C | T | 1 | a0001c0001t0003g0173 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.1154-117G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 8/17 | chr19 | 46727663 | |||||||
chr19:46727689 | C | T | 1 | a0001c0006t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1154-143G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 8/17 | chr19 | 46727689 | |||||||
chr19:46727841 | C | A | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.1153+53G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 8/17 | chr19 | 46727841 | |||||||
chr19:46728135 | G | A | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0121 |
3 | NA18948.hp1 NA18963.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.1040-128C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 7/17 | chr19 | 46728135 | |||||||
chr19:46728215 | C | G | 1 | a0001c0002t0004g0068 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.1040-208G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 7/17 | chr19 | 46728215 | |||||||
chr19:46728349 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1039+269G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 7/17 | chr19 | 46728349 | |||||||
chr19:46728412 | C | T | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1039+206G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 7/17 | chr19 | 46728412 | |||||||
chr19:46728860 | C | T | 2 | a0001c0002t0001g0057 a0001c0002t0001g0058 |
2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.880-83G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46728860 | |||||||
chr19:46728861 | G | A | 3 | a0002c0003t0001g0123 a0002c0003t0001g0124 a0002c0003t0001g0125 |
3 | HG02486.hp2 HG02717.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.880-84C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46728861 | |||||||
chr19:46728940 | G | GGACAGCT others(10): Show |
1 | a0001c0001t0001g0027 | 2 | HG00673.hp1 HG02129.hp1 |
intron_variant | MODIFIER | c.880-180_880-164dup others(17): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46728940 | |||||||
chr19:46728966 | C | T | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(168): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.880-189G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46728966 | |||||||
chr19:46729085 | G | A | 5 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0085 others(2): Show |
7 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-308C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729085 | |||||||
chr19:46729111 | G | A | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.880-334C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729111 | |||||||
chr19:46729190 | C | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0145 |
2 | HG00741.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.880-413G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729190 | |||||||
chr19:46729281 | C | T | 2 | a0001c0001t0001g0072 a0001c0001t0001g0082 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.880-504G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729281 | |||||||
chr19:46729418 | A | G | 8 | a0001c0001t0002g0030 a0001c0001t0002g0075 a0001c0001t0002g0076 others(5): Show |
9 | HG00621.hp2 NA18612.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.880-641T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729418 | |||||||
chr19:46729455 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.880-678C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729455 | |||||||
chr19:46729491 | G | T | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.880-714C>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729491 | |||||||
chr19:46729601 | G | A | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.880-824C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729601 | |||||||
chr19:46729722 | C | A | 1 | a0002c0003t0001g0236 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.880-945G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729722 | |||||||
chr19:46729887 | A | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(243): Show |
396 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(393): Show |
intron_variant | MODIFIER | c.879+845T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46729887 | |||||||
chr19:46730191 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.879+541C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46730191 | |||||||
chr19:46730233 | G | C | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.879+499C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46730233 | |||||||
chr19:46730421 | GAA | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
147 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(144): Show |
intron_variant | MODIFIER | c.879+309_879+310del others(2): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46730421 | |||||||
chr19:46730652 | G | A | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 |
3 | HG02818.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.879+80C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46730652 | |||||||
chr19:46730674 | G | C | 1 | a0001c0001t0002g0104 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.879+58C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 6/17 | chr19 | 46730674 | |||||||
chr19:46731087 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.738-214G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731087 | |||||||
chr19:46731096 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.738-223C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731096 | |||||||
chr19:46731276 | T | C | 1 | a0001c0001t0003g0182 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.738-403A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731276 | |||||||
chr19:46731319 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.738-446G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731319 | |||||||
chr19:46731356 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.738-483G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731356 | |||||||
chr19:46731362 | T | A | 1 | a0001c0001t0001g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.738-489A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731362 | |||||||
chr19:46731416 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.738-543G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731416 | |||||||
chr19:46731536 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.738-663A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731536 | |||||||
chr19:46731628 | G | A | 18 | a0001c0002t0001g0005 a0001c0002t0001g0008 a0001c0002t0001g0054 others(15): Show |
36 | HG00280.hp1 HG00323.hp2 HG00423.hp2 others(33): Show |
intron_variant | MODIFIER | c.738-755C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731628 | |||||||
chr19:46731718 | A | G | 1 | a0001c0001t0001g0133 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.738-845T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46731718 | |||||||
chr19:46732034 | C | A | 1 | a0001c0002t0004g0116 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.737+1005G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732034 | |||||||
chr19:46732132 | C | T | 1 | a0001c0001t0002g0089 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.737+907G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732132 | |||||||
chr19:46732373 | C | T | 2 | a0001c0001t0001g0204 a0001c0001t0012g0131 |
2 | HG01433.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.737+666G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732373 | |||||||
chr19:46732444 | T | G | 2 | a0001c0001t0003g0044 a0001c0001t0003g0183 |
3 | HG02145.hp2 HG02572.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.737+595A>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732444 | |||||||
chr19:46732458 | C | T | 99 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(96): Show |
151 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(148): Show |
intron_variant | MODIFIER | c.737+581G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732458 | |||||||
chr19:46732459 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.737+580C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732459 | |||||||
chr19:46732529 | T | C | 1 | a0001c0006t0001g0235 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.737+510A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732529 | |||||||
chr19:46732564 | C | T | 1 | a0001c0001t0003g0172 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.737+475G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732564 | |||||||
chr19:46732634 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.737+405G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732634 | |||||||
chr19:46732773 | G | A | 4 | a0001c0001t0001g0162 a0001c0002t0001g0056 a0001c0002t0001g0059 others(1): Show |
4 | HG00741.hp1 HG01358.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.737+266C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732773 | |||||||
chr19:46732831 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.737+208A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732831 | |||||||
chr19:46732835 | G | A | 1 | a0002c0003t0001g0206 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.737+204C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732835 | |||||||
chr19:46732959 | A | G | 13 | a0001c0004t0001g0013 a0001c0004t0001g0026 a0001c0004t0001g0239 others(10): Show |
19 | HG00544.hp2 HG00609.hp2 HG01069.hp1 others(16): Show |
intron_variant | MODIFIER | c.737+80T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46732959 | |||||||
chr19:46733011 | G | C | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
158 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.737+28C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 5/17 | chr19 | 46733011 | |||||||
chr19:46733465 | T | C | 2 | a0002c0003t0006g0062 a0002c0003t0006g0063 |
2 | NA18985.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.540-229A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46733465 | |||||||
chr19:46733526 | T | C | 25 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0047 others(22): Show |
30 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.540-290A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46733526 | |||||||
chr19:46733586 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.540-350G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46733586 | |||||||
chr19:46733690 | G | A | 1 | a0001c0001t0002g0028 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.540-454C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46733690 | |||||||
chr19:46733736 | C | T | 2 | a0001c0001t0001g0133 a0001c0001t0001g0134 |
2 | HG01884.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.540-500G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46733736 | |||||||
chr19:46733783 | G | A | 2 | a0001c0001t0001g0135 a0001c0001t0001g0164 |
2 | HG02723.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.540-547C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46733783 | |||||||
chr19:46734032 | T | A | 1 | a0001c0001t0002g0076 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.540-796A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734032 | |||||||
chr19:46734046 | G | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0082 |
2 | HG02738.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.540-810C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734046 | |||||||
chr19:46734078 | G | A | 28 | a0001c0001t0001g0045 a0001c0001t0001g0191 a0001c0010t0001g0203 others(25): Show |
34 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(31): Show |
intron_variant | MODIFIER | c.540-842C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734078 | |||||||
chr19:46734148 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.540-912C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734148 | |||||||
chr19:46734218 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.540-982A>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734218 | |||||||
chr19:46734278 | G | C | 31 | a0001c0001t0003g0016 a0001c0001t0003g0021 a0001c0001t0003g0022 others(28): Show |
42 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(39): Show |
intron_variant | MODIFIER | c.540-1042C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734278 | |||||||
chr19:46734294 | T | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(8): Show |
24 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.540-1058A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734294 | |||||||
chr19:46734483 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.540-1247A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734483 | |||||||
chr19:46734551 | T | C | 3 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0087 |
3 | HG02818.hp2 HG03195.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.540-1315A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734551 | |||||||
chr19:46734594 | C | T | 7 | a0001c0001t0001g0041 a0001c0001t0001g0151 a0001c0005t0001g0018 others(4): Show |
10 | HG02280.hp2 HG02572.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.540-1358G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734594 | |||||||
chr19:46734734 | G | C | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.540-1498C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734734 | |||||||
chr19:46734790 | G | C | 1 | a0001c0006t0001g0074 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.540-1554C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734790 | |||||||
chr19:46734810 | A | G | 182 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(179): Show |
278 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(275): Show |
intron_variant | MODIFIER | c.540-1574T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734810 | |||||||
chr19:46734814 | G | A | 2 | a0002c0003t0001g0199 a0002c0003t0001g0202 |
2 | HG03471.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.540-1578C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734814 | |||||||
chr19:46734825 | C | T | 1 | a0001c0001t0002g0028 | 2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.540-1589G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734825 | |||||||
chr19:46734910 | C | T | 2 | a0001c0005t0001g0050 a0001c0005t0001g0051 |
2 | HG02280.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.540-1674G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734910 | |||||||
chr19:46734982 | A | C | 5 | a0001c0001t0002g0028 a0001c0001t0002g0029 a0001c0001t0002g0085 others(2): Show |
7 | HG02486.hp1 HG02615.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.540-1746T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46734982 | |||||||
chr19:46735165 | G | A | 1 | a0001c0001t0007g0105 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.539+1658C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46735165 | |||||||
chr19:46735326 | A | T | 1 | a0002c0003t0001g0209 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.539+1497T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46735326 | |||||||
chr19:46735402 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
158 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.539+1421C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46735402 | |||||||
chr19:46735692 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0045 others(24): Show |
47 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(44): Show |
intron_variant | MODIFIER | c.539+1131G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46735692 | |||||||
chr19:46735989 | T | C | 3 | a0001c0001t0001g0043 a0001c0001t0001g0225 a0004c0013t0001g0220 |
4 | HG01257.hp1 HG01978.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.539+834A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46735989 | |||||||
chr19:46736132 | G | A | 1 | a0001c0001t0001g0153 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.539+691C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736132 | |||||||
chr19:46736239 | T | C | 2 | a0001c0001t0001g0164 a0001c0001t0001g0170 |
2 | HG02055.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.539+584A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736239 | |||||||
chr19:46736504 | TA | T | 12 | a0001c0001t0001g0087 a0001c0001t0001g0107 a0001c0001t0001g0146 others(9): Show |
14 | HG01070.hp2 HG01257.hp2 HG02040.hp1 others(11): Show |
intron_variant | MODIFIER | c.539+318delT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736504 | |||||||
chr19:46736504 | TAA | T | 156 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(153): Show |
258 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(255): Show |
intron_variant | MODIFIER | c.539+317_539+318del others(2): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736504 | |||||||
chr19:46736504 | TAAA | T | 40 | a0001c0001t0001g0046 a0001c0001t0001g0135 a0001c0001t0001g0150 others(37): Show |
52 | HG00597.hp2 HG00609.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.539+316_539+318del others(3): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736504 | |||||||
chr19:46736552 | C | CA | 35 | a0001c0001t0001g0034 a0001c0001t0001g0066 a0001c0001t0001g0106 others(32): Show |
38 | HG00544.hp2 HG01175.hp2 HG01243.hp2 others(35): Show |
intron_variant | MODIFIER | c.539+270dupT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736552 | |||||||
chr19:46736552 | CA | C | 40 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0017 others(37): Show |
67 | HG00140.hp1 HG00558.hp1 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.539+270delT | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736552 | |||||||
chr19:46736552 | CAA | C | 56 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0041 others(53): Show |
79 | HG00597.hp2 HG00609.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.539+269_539+270del others(2): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736552 | |||||||
chr19:46736606 | A | C | 3 | a0001c0001t0002g0075 a0001c0001t0002g0076 a0001c0001t0002g0121 |
3 | NA18948.hp1 NA18963.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.539+217T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736606 | |||||||
chr19:46736636 | G | C | 1 | a0001c0001t0001g0112 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.539+187C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736636 | |||||||
chr19:46736662 | G | C | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
159 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.539+161C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736662 | |||||||
chr19:46736715 | T | C | 1 | a0001c0002t0001g0008 | 5 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(2): Show |
intron_variant | MODIFIER | c.539+108A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736715 | |||||||
chr19:46736738 | C | T | 1 | a0002c0003t0001g0208 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.539+85G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 4/17 | chr19 | 46736738 | |||||||
chr19:46736918 | C | T | 1 | a0002c0003t0001g0236 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.461-17G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46736918 | |||||||
chr19:46737092 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.461-191A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737092 | |||||||
chr19:46737190 | G | A | 25 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0047 others(22): Show |
30 | HG00733.hp1 HG00738.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.461-289C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737190 | |||||||
chr19:46737251 | G | A | 1 | a0001c0001t0002g0113 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.461-350C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737251 | |||||||
chr19:46737298 | C | A | 2 | a0001c0001t0001g0195 a0001c0001t0001g0234 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.461-397G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737298 | |||||||
chr19:46737572 | C | T | 11 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0199 others(8): Show |
15 | HG00733.hp1 HG01074.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.460+592G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737572 | |||||||
chr19:46737619 | G | A | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.460+545C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737619 | |||||||
chr19:46737766 | C | T | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.460+398G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737766 | |||||||
chr19:46737871 | C | T | 5 | a0001c0006t0001g0065 a0001c0006t0001g0067 a0001c0006t0001g0073 others(2): Show |
5 | HG01261.hp1 HG02145.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.460+293G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737871 | |||||||
chr19:46737933 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0232 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.460+231C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737933 | |||||||
chr19:46737960 | G | A | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.460+204C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 3/17 | chr19 | 46737960 | |||||||
chr19:46738342 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(8): Show |
24 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.387-105G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738342 | |||||||
chr19:46738346 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.387-109G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738346 | |||||||
chr19:46738358 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.387-121A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738358 | |||||||
chr19:46738377 | C | A | 1 | a0001c0001t0002g0119 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.387-140G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738377 | |||||||
chr19:46738402 | C | T | 103 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(100): Show |
162 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(159): Show |
intron_variant | MODIFIER | c.387-165G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738402 | |||||||
chr19:46738513 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386+272G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738513 | |||||||
chr19:46738591 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.386+194T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738591 | |||||||
chr19:46738711 | C | T | 1 | a0001c0001t0002g0071 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.386+74G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 2/17 | chr19 | 46738711 | |||||||
chr19:46738895 | G | A | 32 | a0001c0001t0003g0016 a0001c0001t0003g0021 a0001c0001t0003g0022 others(29): Show |
43 | HG00597.hp2 HG00609.hp1 HG01081.hp1 others(40): Show |
splice_region_variant&intron_variant | LOW | c.283-7C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46738895 | |||||||
chr19:46739113 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283-225C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739113 | |||||||
chr19:46739165 | C | T | 1 | a0001c0004t0001g0239 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.283-277G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739165 | |||||||
chr19:46739190 | C | T | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283-302G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739190 | |||||||
chr19:46739437 | G | A | 1 | a0001c0002t0004g0068 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.283-549C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739437 | |||||||
chr19:46739484 | C | T | 1 | a0001c0001t0002g0070 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.283-596G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739484 | |||||||
chr19:46739490 | C | T | 1 | a0002c0003t0001g0199 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.283-602G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739490 | |||||||
chr19:46739543 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.283-655G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739543 | |||||||
chr19:46739686 | G | A | 1 | a0001c0004t0001g0245 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.283-798C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739686 | |||||||
chr19:46739735 | G | A | 54 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0045 others(51): Show |
79 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.283-847C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739735 | |||||||
chr19:46739825 | G | A | 14 | a0002c0003t0001g0047 a0002c0003t0001g0123 a0002c0003t0001g0124 others(11): Show |
15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.283-937C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739825 | |||||||
chr19:46739975 | C | G | 1 | a0001c0007t0001g0139 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.283-1087G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46739975 | |||||||
chr19:46740121 | T | C | 1 | a0005c0009t0001g0120 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.283-1233A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46740121 | |||||||
chr19:46740250 | C | G | 1 | a0001c0004t0001g0239 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.283-1362G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46740250 | |||||||
chr19:46740341 | T | C | 2 | a0001c0001t0001g0189 a0001c0001t0001g0232 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.283-1453A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46740341 | |||||||
chr19:46740364 | A | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(8): Show |
24 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.283-1476T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46740364 | |||||||
chr19:46740371 | T | G | 2 | a0001c0001t0001g0189 a0001c0001t0001g0232 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.283-1483A>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46740371 | |||||||
chr19:46740497 | C | T | 1 | a0001c0010t0001g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283-1609G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46740497 | |||||||
chr19:46741166 | A | G | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.283-2278T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741166 | |||||||
chr19:46741215 | C | A | 1 | a0001c0001t0001g0130 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.283-2327G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741215 | |||||||
chr19:46741219 | A | C | 1 | a0001c0004t0001g0247 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.283-2331T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741219 | |||||||
chr19:46741273 | C | A | 102 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(99): Show |
161 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(158): Show |
intron_variant | MODIFIER | c.283-2385G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741273 | |||||||
chr19:46741444 | G | C | 1 | a0001c0001t0003g0185 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.283-2556C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741444 | |||||||
chr19:46741491 | C | T | 1 | a0001c0004t0001g0246 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.283-2603G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741491 | |||||||
chr19:46741544 | C | T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0138 |
2 | HG03453.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.283-2656G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741544 | |||||||
chr19:46741614 | A | C | 1 | a0001c0001t0002g0069 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.283-2726T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741614 | |||||||
chr19:46741615 | T | A | 1 | a0001c0001t0003g0186 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.283-2727A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741615 | |||||||
chr19:46741648 | C | A | 1 | a0001c0001t0001g0204 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.283-2760G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741648 | |||||||
chr19:46741651 | A | G | 2 | a0001c0001t0001g0040 a0001c0001t0001g0137 |
3 | HG00673.hp2 NA18948.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.283-2763T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741651 | |||||||
chr19:46741781 | G | A | 1 | a0001c0001t0003g0186 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.283-2893C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741781 | |||||||
chr19:46741828 | C | T | 15 | a0001c0001t0001g0006 a0001c0001t0001g0040 a0001c0001t0001g0048 others(12): Show |
23 | HG00673.hp2 HG00735.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.283-2940G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46741828 | |||||||
chr19:46742002 | G | A | 1 | a0001c0001t0003g0188 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.283-3114C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742002 | |||||||
chr19:46742035 | C | CTCAAAAA others(3): Show |
1 | a0001c0002t0004g0068 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.283-3157_283-3148d others(12): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742035 | |||||||
chr19:46742228 | C | T | 11 | a0002c0003t0001g0023 a0002c0003t0001g0024 a0002c0003t0001g0199 others(8): Show |
15 | HG00733.hp1 HG01074.hp2 HG02083.hp1 others(12): Show |
intron_variant | MODIFIER | c.283-3340G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742228 | |||||||
chr19:46742242 | G | A | 3 | a0002c0003t0001g0205 a0002c0003t0001g0206 a0002c0003t0001g0236 |
3 | HG02083.hp1 NA18963.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.283-3354C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742242 | |||||||
chr19:46742535 | T | C | 157 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.282+3614A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742535 | |||||||
chr19:46742548 | T | C | 1 | a0001c0001t0003g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.282+3601A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742548 | |||||||
chr19:46742797 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0197 |
2 | HG02886.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.282+3352C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742797 | |||||||
chr19:46742851 | G | A | 2 | a0001c0001t0001g0187 a0001c0001t0003g0188 |
2 | HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.282+3298C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742851 | |||||||
chr19:46742871 | T | C | 1 | a0001c0001t0002g0121 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.282+3278A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742871 | |||||||
chr19:46742973 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3176A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742973 | |||||||
chr19:46742975 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3174C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742975 | |||||||
chr19:46742976 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3173T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742976 | |||||||
chr19:46742980 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3169T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742980 | |||||||
chr19:46742982 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3167A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742982 | |||||||
chr19:46742984 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3165A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742984 | |||||||
chr19:46742985 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3164T>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742985 | |||||||
chr19:46742989 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3160C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742989 | |||||||
chr19:46742990 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3159A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742990 | |||||||
chr19:46742991 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3158G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742991 | |||||||
chr19:46742995 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3154G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742995 | |||||||
chr19:46742998 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3151G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46742998 | |||||||
chr19:46743001 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3148C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743001 | |||||||
chr19:46743002 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3147C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743002 | |||||||
chr19:46743003 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3146C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743003 | |||||||
chr19:46743004 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3145A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743004 | |||||||
chr19:46743009 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3140G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743009 | |||||||
chr19:46743010 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3139A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743010 | |||||||
chr19:46743013 | A | T | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3136T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743013 | |||||||
chr19:46743014 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3135A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743014 | |||||||
chr19:46743016 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3133T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743016 | |||||||
chr19:46743018 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3131G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743018 | |||||||
chr19:46743019 | T | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3130A>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743019 | |||||||
chr19:46743020 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3129T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743020 | |||||||
chr19:46743021 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3128A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743021 | |||||||
chr19:46743024 | T | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3125A>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743024 | |||||||
chr19:46743026 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3123G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743026 | |||||||
chr19:46743030 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3119G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743030 | |||||||
chr19:46743033 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3116G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743033 | |||||||
chr19:46743035 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3114G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743035 | |||||||
chr19:46743038 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3111C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743038 | |||||||
chr19:46743039 | G | A | 2 | a0001c0001t0001g0189 a0001c0001t0001g0232 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.282+3110C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743039 | |||||||
chr19:46743040 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3109C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743040 | |||||||
chr19:46743041 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3108T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743041 | |||||||
chr19:46743046 | A | G | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3103T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743046 | |||||||
chr19:46743047 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.282+3102A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743047 | |||||||
chr19:46743233 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.282+2916A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743233 | |||||||
chr19:46743328 | A | T | 1 | a0001c0001t0003g0136 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.282+2821T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743328 | |||||||
chr19:46743429 | G | C | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.282+2720C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743429 | |||||||
chr19:46743610 | C | T | 1 | a0001c0001t0002g0014 | 4 | NA19000.hp2 NA19063.hp2 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.282+2539G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743610 | |||||||
chr19:46743617 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.282+2532G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743617 | |||||||
chr19:46743691 | G | C | 14 | a0002c0003t0001g0047 a0002c0003t0001g0123 a0002c0003t0001g0124 others(11): Show |
15 | HG00738.hp1 HG01243.hp2 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.282+2458C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743691 | |||||||
chr19:46743722 | A | G | 1 | a0001c0001t0001g0039 | 2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.282+2427T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743722 | |||||||
chr19:46743884 | CAG | C | 11 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(8): Show |
24 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.282+2263_282+2264d others(4): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743884 | |||||||
chr19:46743918 | AAAATAAA others(5): Show |
A | 1 | a0001c0005t0001g0053 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.282+2219_282+2230d others(14): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743918 | |||||||
chr19:46743933 | A | G | 1 | a0001c0002t0001g0054 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.282+2216T>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743933 | |||||||
chr19:46743942 | T | C | 1 | a0001c0002t0001g0061 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.282+2207A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46743942 | |||||||
chr19:46744293 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.282+1856A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744293 | |||||||
chr19:46744400 | T | C | 1 | a0001c0001t0001g0046 | 2 | HG00642.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.282+1749A>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744400 | |||||||
chr19:46744524 | C | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(21): Show |
43 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.282+1625G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744524 | |||||||
chr19:46744529 | G | A | 100 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(97): Show |
158 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(155): Show |
intron_variant | MODIFIER | c.282+1620C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744529 | |||||||
chr19:46744543 | C | G | 2 | a0001c0006t0001g0065 a0001c0006t0001g0067 |
2 | HG02965.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.282+1606G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744543 | |||||||
chr19:46744839 | C | G | 2 | a0001c0001t0001g0066 a0001c0001t0005g0038 |
3 | HG01070.hp1 HG01071.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.282+1310G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744839 | |||||||
chr19:46744944 | G | A | 3 | a0001c0002t0004g0010 a0001c0002t0004g0037 a0001c0002t0004g0127 |
8 | HG00423.hp2 HG00621.hp1 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+1205C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46744944 | |||||||
chr19:46745051 | G | A | 24 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(21): Show |
43 | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(40): Show |
intron_variant | MODIFIER | c.282+1098C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745051 | |||||||
chr19:46745233 | C | G | 1 | a0001c0006t0001g0065 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.282+916G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745233 | |||||||
chr19:46745328 | C | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0064 others(8): Show |
24 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(21): Show |
intron_variant | MODIFIER | c.282+821G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745328 | |||||||
chr19:46745556 | A | T | 1 | a0001c0001t0001g0045 | 2 | HG02258.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.282+593T>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745556 | |||||||
chr19:46745563 | C | T | 1 | a0001c0001t0001g0191 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.282+586G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745563 | |||||||
chr19:46745619 | G | A | 1 | a0001c0008t0002g0128 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.282+530C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745619 | |||||||
chr19:46745722 | C | G | 101 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(98): Show |
159 | HG00140.hp1 HG00544.hp1 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.282+427G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745722 | |||||||
chr19:46745789 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+360C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745789 | |||||||
chr19:46745993 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.282+156G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46745993 | |||||||
chr19:46746008 | C | G | 1 | a0001c0001t0012g0131 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.282+141G>C | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746008 | |||||||
chr19:46746020 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.282+129C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746020 | |||||||
chr19:46746021 | G | A | 10 | a0002c0003t0001g0047 a0002c0003t0001g0208 a0002c0003t0001g0209 others(7): Show |
11 | HG01243.hp2 HG01884.hp1 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.282+128C>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746021 | |||||||
chr19:46746031 | G | GC | 32 | a0001c0001t0001g0017 a0001c0001t0001g0048 a0001c0001t0001g0130 others(29): Show |
39 | HG00544.hp2 HG00597.hp2 HG01192.hp2 others(36): Show |
intron_variant | MODIFIER | c.282+117dupG | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746031 | |||||||
chr19:46746037 | C | A | 1 | a0001c0001t0003g0238 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.282+112G>T | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746037 | |||||||
chr19:46746039 | G | C | 153 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(150): Show |
237 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.282+110C>G | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746039 | |||||||
chr19:46746040 | C | T | 2 | a0002c0003t0006g0062 a0002c0003t0006g0063 |
2 | NA18985.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.282+109G>A | STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746040 | |||||||
chr19:46746094 | A | AGGCCG | 11 | a0001c0001t0001g0055 a0001c0002t0001g0005 a0001c0002t0001g0008 others(8): Show |
24 | HG00280.hp1 HG00323.hp2 HG00639.hp2 others(21): Show |
intron_variant | MODIFIER | c.282+50_282+54dupCG others(3): Show |
STRN4 | ENSG00000090372.15 | transcript | ENST00000263280.11 | protein_coding | 1/17 | chr19 | 46746094 |