Item | Value |
---|---|
geneid | 27020 |
ensemblid | ENSG00000156642.17 |
hgncid | 17867 |
symbol | NPTN |
name | neuroplastin |
refseq_nuc | NM_012428.4 |
refseq_prot | NP_036560.1 |
ensembl_nuc | ENST00000345330.9 |
ensembl_prot | ENSP00000290401.4 |
mane_status | MANE Select |
chr | chr15 |
start | 73560014 |
end | 73633389 |
strand | - |
ver | v1.2 |
region | chr15:73560014-73633389 |
region5000 | chr15:73555014-73638389 |
regionname0 | NPTN_chr15_73560014_73633389 |
regionname5000 | NPTN_chr15_73555014_73638389 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1194 | 340 | 76 | 58 | 162 | 8 | 34 | NPTN_chr15_73555014_73638389 | NPTN | ATGTC others(1189): Show |
chr15 | 73555014 | 73638389 | ||
a0001c0002 | 0/0 | 1194 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | ATGTC others(1189): Show |
chr15 | 73555014 | 73638389 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2420 | 319 | 74 | 57 | 146 | 6 | 34 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
a0001c0001t0002 | 0/0 | 2420 | 15 | 0 | 0 | 13 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
a0001c0001t0003 | 0/0 | 2420 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
a0001c0001t0004 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
a0001c0001t0005 | 0/0 | 2420 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
a0001c0001t0006 | 0/0 | 2420 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
a0001c0002t0001 | 0/0 | 2420 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | GAGGC others(2415): Show |
chr15 | 73555014 | 73638389 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 9 | 0 | 3 | 4 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0002 | 0/0 | 6 | 0 | 0 | 4 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0004 | 1/0 | 4 | 3 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0005 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0247 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0005g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0001t0006g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0002t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
a0001c0002t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0009 | EUR | FIN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | FIN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CHS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01346 | hp2 | a0001 | c0001 | t0006 | g0279 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0208 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0030 | EUR | IBS | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0198 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CDX | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0216 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02280 | hp1 | a0001 | c0002 | t0001 | g0273 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0205 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0263 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0274 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0237 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0206 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | MSL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0051 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0017 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0203 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0188 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0201 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0275 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0017 | SAS | STU | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | CHB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0041 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0040 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19056 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | YRI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | TSI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | GIH | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0018 | SAS | GIH | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20300 | hp1 | a0001 | c0001 | t0005 | g0261 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | USA | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0272 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0247 | REF | REF | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0004 | REF | REF | NPTN_chr15_73555014_73638389 | NPTN | chr15 | 73555014 | 73638389 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73570265 | C | T | 1 | a0001c0002 | 2 | HG02280.hp1 HG02922.hp1 |
synonymous_variant | LOW | c.999G>A | p.Val333Val | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/9 | 1173/2420 | 999/1197 | 333/398 | chr15 | 73570265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73560123 | C | T | 1 | a0001c0001t0005 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*940G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 9/9 | 1787 | chr15 | 73560123 | ||||||
chr15:73560367 | A | G | 1 | a0001c0001t0004 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*696T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 9/9 | 1543 | chr15 | 73560367 | ||||||
chr15:73560948 | G | A | 1 | a0001c0001t0002 | 15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*115C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 9/9 | 962 | chr15 | 73560948 | ||||||
chr15:73633294 | G | C | 1 | a0001c0001t0006 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/9 | 79 | chr15 | 73633294 | ||||||
chr15:73633354 | C | T | 1 | a0001c0001t0003 | 3 | NA18965.hp2 NA18994.hp1 NA19002.hp2 |
5_prime_UTR_variant | MODIFIER | c.-139G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/9 | 139 | chr15 | 73633354 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr15:73561145 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.*15-97C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561145 | |||||||
chr15:73561409 | T | C | 1 | a0001c0001t0002g0219 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.*15-361A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561409 | |||||||
chr15:73561454 | C | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.*15-406G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561454 | |||||||
chr15:73561455 | G | A | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.*15-407C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561455 | |||||||
chr15:73561468 | T | C | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.*15-420A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561468 | |||||||
chr15:73561661 | T | C | 1 | a0001c0001t0001g0240 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.*14+235A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561661 | |||||||
chr15:73561740 | A | G | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.*14+156T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 8/8 | chr15 | 73561740 | |||||||
chr15:73562191 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1137-221A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562191 | |||||||
chr15:73562249 | A | C | 1 | a0001c0001t0001g0179 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1137-279T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562249 | |||||||
chr15:73562268 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1137-298G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562268 | |||||||
chr15:73562610 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1136+626A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562610 | |||||||
chr15:73562657 | G | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0046 others(12): Show |
18 | HG01496.hp2 HG02055.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.1136+579C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562657 | |||||||
chr15:73562702 | T | C | 77 | a0001c0001t0001g0005 a0001c0001t0001g0010 a0001c0001t0001g0034 others(74): Show |
93 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.1136+534A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562702 | |||||||
chr15:73562896 | G | C | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1136+340C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562896 | |||||||
chr15:73562989 | G | GA | 32 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(29): Show |
37 | HG00558.hp1 HG00639.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1136+246dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73562989 | |||||||
chr15:73563014 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1136+222C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73563014 | |||||||
chr15:73563173 | A | C | 1 | a0001c0001t0001g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1136+63T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 7/8 | chr15 | 73563173 | |||||||
chr15:73563297 | A | G | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1115-40T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563297 | |||||||
chr15:73563706 | C | T | 1 | a0001c0001t0001g0257 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1115-449G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563706 | |||||||
chr15:73563735 | A | G | 1 | a0001c0001t0001g0179 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.1115-478T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563735 | |||||||
chr15:73563748 | T | G | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1115-491A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563748 | |||||||
chr15:73563844 | A | G | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1115-587T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563844 | |||||||
chr15:73563962 | C | A | 1 | a0001c0001t0001g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1115-705G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73563962 | |||||||
chr15:73564104 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1115-847T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564104 | |||||||
chr15:73564501 | C | A | 1 | a0001c0001t0001g0185 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1115-1244G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564501 | |||||||
chr15:73564529 | T | C | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1115-1272A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564529 | |||||||
chr15:73564658 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1115-1401T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564658 | |||||||
chr15:73564707 | C | A | 17 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 others(14): Show |
24 | HG01346.hp1 HG01516.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1115-1450G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564707 | |||||||
chr15:73564739 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1115-1482G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564739 | |||||||
chr15:73564995 | A | T | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.1115-1738T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73564995 | |||||||
chr15:73565065 | G | T | 1 | a0001c0001t0001g0021 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1115-1808C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565065 | |||||||
chr15:73565250 | C | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.1115-1993G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565250 | |||||||
chr15:73565822 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1115-2565C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565822 | |||||||
chr15:73565885 | T | C | 17 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 others(14): Show |
24 | HG01346.hp1 HG01516.hp1 HG01517.hp2 others(21): Show |
intron_variant | MODIFIER | c.1115-2628A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565885 | |||||||
chr15:73565899 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1115-2642G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73565899 | |||||||
chr15:73566074 | A | G | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
122 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.1115-2817T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566074 | |||||||
chr15:73566279 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1115-3022C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566279 | |||||||
chr15:73566296 | T | C | 2 | a0001c0001t0001g0156 a0001c0001t0001g0275 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1115-3039A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566296 | |||||||
chr15:73566506 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0277 a0001c0001t0001g0278 |
4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1115-3249A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566506 | |||||||
chr15:73566524 | A | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1115-3267T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566524 | |||||||
chr15:73566675 | A | C | 85 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(82): Show |
108 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.1115-3418T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566675 | |||||||
chr15:73566786 | G | C | 1 | a0001c0001t0001g0243 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1114+3364C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566786 | |||||||
chr15:73566842 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1114+3308C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566842 | |||||||
chr15:73566967 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+3183C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73566967 | |||||||
chr15:73567001 | GCTTTT | G | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+3144_1114+314 others(9): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567001 | |||||||
chr15:73567002 | C | CT | 5 | a0001c0001t0001g0005 a0001c0001t0001g0076 a0001c0001t0001g0230 others(2): Show |
8 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.1114+3147dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | |||||||
chr15:73567002 | CT | C | 190 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(187): Show |
228 | HG00280.hp1 HG00438.hp2 HG00544.hp1 others(225): Show |
intron_variant | MODIFIER | c.1114+3147delA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | |||||||
chr15:73567002 | CTT | C | 10 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0015 others(7): Show |
10 | HG00642.hp1 HG01069.hp2 HG01346.hp1 others(7): Show |
intron_variant | MODIFIER | c.1114+3146_1114+314 others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | |||||||
chr15:73567002 | CTTTT | C | 44 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(41): Show |
50 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.1114+3144_1114+314 others(8): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567002 | |||||||
chr15:73567128 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1114+3022A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567128 | |||||||
chr15:73567147 | T | A | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(94): Show |
121 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.1114+3003A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567147 | |||||||
chr15:73567166 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1114+2984A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567166 | |||||||
chr15:73567221 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+2929A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567221 | |||||||
chr15:73567234 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+2916T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567234 | |||||||
chr15:73567315 | G | T | 1 | a0001c0001t0001g0029 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1114+2835C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567315 | |||||||
chr15:73567514 | G | A | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
217 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.1114+2636C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567514 | |||||||
chr15:73567531 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1114+2619A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567531 | |||||||
chr15:73567628 | CT | C | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+2521delA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567628 | |||||||
chr15:73567813 | G | A | 1 | a0001c0001t0001g0014 | 2 | HG00733.hp2 HG00735.hp2 |
intron_variant | MODIFIER | c.1114+2337C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567813 | |||||||
chr15:73567902 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1114+2248G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567902 | |||||||
chr15:73567952 | G | A | 1 | a0001c0001t0001g0157 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1114+2198C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567952 | |||||||
chr15:73567977 | A | G | 60 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(57): Show |
69 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(66): Show |
intron_variant | MODIFIER | c.1114+2173T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73567977 | |||||||
chr15:73568019 | C | T | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.1114+2131G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568019 | |||||||
chr15:73568141 | T | TG | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+2008dupC | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568141 | |||||||
chr15:73568148 | A | G | 49 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
55 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1114+2002T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568148 | |||||||
chr15:73568162 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1114+1988A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568162 | |||||||
chr15:73568163 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1114+1987G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568163 | |||||||
chr15:73568194 | T | C | 3 | a0001c0001t0001g0039 a0001c0001t0001g0277 a0001c0001t0001g0278 |
4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.1114+1956A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568194 | |||||||
chr15:73568206 | G | T | 1 | a0001c0001t0001g0103 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1114+1944C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568206 | |||||||
chr15:73568306 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1114+1844G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568306 | |||||||
chr15:73568699 | G | C | 7 | a0001c0001t0001g0038 a0001c0001t0001g0248 a0001c0001t0001g0250 others(4): Show |
8 | HG02015.hp2 HG02083.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.1114+1451C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73568699 | |||||||
chr15:73569032 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1114+1118A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569032 | |||||||
chr15:73569103 | C | T | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.1114+1047G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569103 | |||||||
chr15:73569180 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1114+970G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569180 | |||||||
chr15:73569217 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1114+933C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569217 | |||||||
chr15:73569299 | C | G | 1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1114+851G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569299 | |||||||
chr15:73569300 | G | C | 4 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0249 others(1): Show |
6 | NA18969.hp1 NA18984.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.1114+850C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569300 | |||||||
chr15:73569562 | C | T | 1 | a0001c0001t0001g0029 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1114+588G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569562 | |||||||
chr15:73569571 | A | C | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1114+579T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569571 | |||||||
chr15:73569911 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1114+239T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569911 | |||||||
chr15:73569964 | TAAAATA | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1114+180_1114+185d others(8): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569964 | |||||||
chr15:73569995 | C | A | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(58): Show |
81 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.1114+155G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 6/8 | chr15 | 73569995 | |||||||
chr15:73570426 | G | A | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
splice_region_variant&intron_variant | LOW | c.841-3C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570426 | |||||||
chr15:73570729 | TAAGAAAC others(6): Show |
T | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.841-319_841-307del others(13): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570729 | |||||||
chr15:73570773 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.841-350G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570773 | |||||||
chr15:73570861 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.841-438C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73570861 | |||||||
chr15:73571285 | G | T | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(225): Show |
281 | HG00280.hp1 HG00280.hp2 HG00438.hp2 others(278): Show |
intron_variant | MODIFIER | c.841-862C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571285 | |||||||
chr15:73571416 | C | T | 1 | a0001c0001t0001g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.841-993G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571416 | |||||||
chr15:73571584 | A | G | 6 | a0001c0001t0001g0118 a0001c0001t0001g0128 a0001c0001t0001g0129 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.841-1161T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571584 | |||||||
chr15:73571659 | G | A | 1 | a0001c0001t0001g0113 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.841-1236C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73571659 | |||||||
chr15:73572334 | C | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.840+1328G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572334 | |||||||
chr15:73572335 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0022 others(95): Show |
116 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.840+1327C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572335 | |||||||
chr15:73572490 | C | T | 34 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(31): Show |
40 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.840+1172G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572490 | |||||||
chr15:73572522 | CCCTTGGG others(73): Show |
C | 2 | a0001c0001t0001g0006 a0001c0001t0001g0068 |
4 | NA18960.hp2 NA19007.hp2 NA19075.hp1 others(1): Show |
intron_variant | MODIFIER | c.840+1060_840+1139d others(82): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572522 | |||||||
chr15:73572800 | G | T | 6 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
7 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.840+862C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572800 | |||||||
chr15:73572862 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.840+800C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572862 | |||||||
chr15:73572867 | A | T | 1 | a0001c0001t0001g0184 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.840+795T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73572867 | |||||||
chr15:73573228 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.840+434G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573228 | |||||||
chr15:73573326 | TA | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.840+335delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573326 | |||||||
chr15:73573455 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.840+207C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573455 | |||||||
chr15:73573623 | A | T | 1 | a0001c0001t0003g0040 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.840+39T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 5/8 | chr15 | 73573623 | |||||||
chr15:73573882 | T | G | 1 | a0001c0001t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.707-87A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73573882 | |||||||
chr15:73574015 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.707-220C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574015 | |||||||
chr15:73574039 | A | C | 1 | a0001c0001t0001g0080 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.707-244T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574039 | |||||||
chr15:73574671 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-876G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574671 | |||||||
chr15:73574693 | G | A | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
6 | HG02155.hp2 HG04184.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.707-898C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574693 | |||||||
chr15:73574883 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.707-1088A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73574883 | |||||||
chr15:73575499 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-1704A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575499 | |||||||
chr15:73575534 | C | T | 1 | a0001c0001t0001g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.707-1739G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575534 | |||||||
chr15:73575544 | G | C | 1 | a0001c0001t0001g0208 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.707-1749C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575544 | |||||||
chr15:73575685 | C | G | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.707-1890G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575685 | |||||||
chr15:73575717 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18974.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.707-1922A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575717 | |||||||
chr15:73575755 | T | G | 2 | a0001c0001t0001g0158 a0001c0001t0001g0213 |
2 | HG02015.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.707-1960A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575755 | |||||||
chr15:73575995 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-2200G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73575995 | |||||||
chr15:73576002 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.707-2207C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576002 | |||||||
chr15:73576355 | GTCTC | G | 9 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.707-2564_707-2561d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576355 | |||||||
chr15:73576395 | C | T | 1 | a0001c0001t0001g0035 | 2 | HG03239.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.707-2600G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576395 | |||||||
chr15:73576475 | T | A | 1 | a0001c0001t0001g0115 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.707-2680A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576475 | |||||||
chr15:73576621 | G | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0199 a0001c0001t0001g0201 others(5): Show |
8 | HG01261.hp2 HG01975.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.707-2826C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576621 | |||||||
chr15:73576768 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.707-2973G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576768 | |||||||
chr15:73576950 | G | A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.707-3155C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73576950 | |||||||
chr15:73577213 | G | A | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.707-3418C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577213 | |||||||
chr15:73577234 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-3439G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577234 | |||||||
chr15:73577426 | G | T | 130 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(127): Show |
165 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(162): Show |
intron_variant | MODIFIER | c.707-3631C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577426 | |||||||
chr15:73577567 | T | C | 173 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(170): Show |
214 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(211): Show |
intron_variant | MODIFIER | c.707-3772A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577567 | |||||||
chr15:73577621 | A | G | 1 | a0001c0001t0001g0210 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.707-3826T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577621 | |||||||
chr15:73577818 | G | A | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.707-4023C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577818 | |||||||
chr15:73577831 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-4036C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577831 | |||||||
chr15:73577951 | T | C | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.707-4156A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577951 | |||||||
chr15:73577953 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0001g0068 a0001c0001t0001g0072 |
5 | NA18960.hp2 NA18986.hp1 NA19007.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-4158A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577953 | |||||||
chr15:73577961 | C | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.707-4166G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73577961 | |||||||
chr15:73578020 | C | G | 1 | a0001c0001t0001g0232 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.707-4225G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578020 | |||||||
chr15:73578105 | C | T | 2 | a0001c0001t0001g0026 a0001c0001t0001g0141 |
3 | NA18952.hp1 NA18986.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.707-4310G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578105 | |||||||
chr15:73578212 | C | T | 1 | a0001c0001t0001g0211 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.707-4417G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578212 | |||||||
chr15:73578229 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.707-4434T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578229 | |||||||
chr15:73578456 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-4661A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578456 | |||||||
chr15:73578460 | T | C | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.707-4665A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578460 | |||||||
chr15:73578681 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-4886G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578681 | |||||||
chr15:73578701 | G | A | 1 | a0001c0001t0001g0183 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.707-4906C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578701 | |||||||
chr15:73578718 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0176 |
2 | HG02615.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.707-4923C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578718 | |||||||
chr15:73578899 | G | A | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.707-5104C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578899 | |||||||
chr15:73578992 | C | CA | 33 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0037 others(30): Show |
37 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(34): Show |
intron_variant | MODIFIER | c.707-5198dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578992 | |||||||
chr15:73578992 | C | CAA | 5 | a0001c0001t0001g0039 a0001c0001t0001g0244 a0001c0001t0001g0270 others(2): Show |
6 | HG01243.hp2 HG01255.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-5199_707-5198d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578992 | |||||||
chr15:73578992 | CA | C | 11 | a0001c0001t0001g0027 a0001c0001t0001g0068 a0001c0001t0001g0073 others(8): Show |
12 | HG01109.hp1 HG01169.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.707-5198delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73578992 | |||||||
chr15:73579144 | T | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.707-5349A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579144 | |||||||
chr15:73579171 | C | T | 14 | a0001c0001t0001g0009 a0001c0001t0001g0019 a0001c0001t0001g0054 others(11): Show |
17 | HG00280.hp1 HG00639.hp2 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.707-5376G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579171 | |||||||
chr15:73579172 | G | A | 2 | a0001c0001t0001g0175 a0001c0001t0001g0189 |
2 | HG01081.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.707-5377C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579172 | |||||||
chr15:73579233 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.707-5438G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579233 | |||||||
chr15:73579277 | CA | C | 149 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(146): Show |
187 | HG00280.hp1 HG00544.hp1 HG00558.hp1 others(184): Show |
intron_variant | MODIFIER | c.707-5483delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579277 | |||||||
chr15:73579441 | A | T | 1 | a0001c0001t0001g0173 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.707-5646T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579441 | |||||||
chr15:73579500 | G | T | 1 | a0001c0001t0001g0278 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.707-5705C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579500 | |||||||
chr15:73579660 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.707-5865C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579660 | |||||||
chr15:73579999 | T | C | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.707-6204A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73579999 | |||||||
chr15:73580158 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.707-6363G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580158 | |||||||
chr15:73580181 | G | A | 1 | a0001c0001t0001g0033 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.707-6386C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580181 | |||||||
chr15:73580230 | G | A | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.707-6435C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580230 | |||||||
chr15:73580271 | G | A | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.707-6476C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580271 | |||||||
chr15:73580400 | T | TTATATAT others(15): Show |
1 | a0001c0001t0001g0178 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.707-6627_707-6606d others(24): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | |||||||
chr15:73580400 | TTATATAT others(4): Show |
T | 32 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(29): Show |
38 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.707-6616_707-6606d others(13): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | |||||||
chr15:73580400 | TTATATAT others(15): Show |
T | 9 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.707-6627_707-6606d others(24): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | |||||||
chr15:73580400 | TTATATAT others(28): Show |
T | 1 | a0001c0002t0001g0274 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.707-6640_707-6606d others(37): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580400 | |||||||
chr15:73580401 | T | TATATATA others(24): Show |
2 | a0001c0001t0001g0026 a0001c0001t0001g0141 |
3 | NA18952.hp1 NA18986.hp2 NA19081.hp1 |
intron_variant | MODIFIER | c.707-6637_707-6607d others(33): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580401 | |||||||
chr15:73580410 | A | T | 1 | a0001c0001t0001g0232 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.707-6615T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580410 | |||||||
chr15:73580411 | A | ATATATAT others(11): Show |
1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.707-6634_707-6617d others(20): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580411 | |||||||
chr15:73580411 | A | ATATATAT others(283): Show |
1 | a0001c0002t0001g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.707-6617_707-6616i others(292): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580411 | |||||||
chr15:73580411 | A | T | 1 | a0001c0001t0001g0002 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.707-6616T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580411 | |||||||
chr15:73580412 | TATATATA others(22): Show |
T | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.707-6646_707-6618d others(31): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580412 | |||||||
chr15:73580419 | ATAATATA others(3): Show |
A | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.707-6634_707-6625d others(12): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580419 | |||||||
chr15:73580421 | A | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.707-6626T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580421 | |||||||
chr15:73580422 | A | T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.707-6627T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580422 | |||||||
chr15:73580430 | ATAATATA others(1): Show |
A | 3 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0129 |
5 | HG00733.hp2 HG00735.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-6643_707-6636d others(10): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580430 | |||||||
chr15:73580432 | A | T | 1 | a0001c0001t0001g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.707-6637T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580432 | |||||||
chr15:73580433 | A | T | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.707-6638T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580433 | |||||||
chr15:73580440 | TA | T | 3 | a0001c0001t0001g0014 a0001c0001t0001g0017 a0001c0001t0001g0129 |
5 | HG00733.hp2 HG00735.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.707-6646delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580440 | |||||||
chr15:73580441 | A | AAT | 109 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(106): Show |
138 | HG00280.hp1 HG00597.hp2 HG00609.hp2 others(135): Show |
intron_variant | MODIFIER | c.707-6648_707-6647d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580441 | |||||||
chr15:73580441 | A | ATAATATA others(13): Show |
4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-6647_707-6646i others(22): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580441 | |||||||
chr15:73580441 | A | T | 48 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
54 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.707-6646T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580441 | |||||||
chr15:73580442 | A | T | 7 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0227 others(4): Show |
10 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.707-6647T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580442 | |||||||
chr15:73580450 | G | A | 7 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0227 others(4): Show |
10 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.707-6655C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580450 | |||||||
chr15:73580451 | T | A | 1 | a0001c0001t0001g0225 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.707-6656A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580451 | |||||||
chr15:73580451 | T | TA | 7 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0227 others(4): Show |
10 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.707-6657dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580451 | |||||||
chr15:73580459 | C | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6664G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580459 | |||||||
chr15:73580460 | A | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6665T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580460 | |||||||
chr15:73580462 | A | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6667T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580462 | |||||||
chr15:73580469 | T | G | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6674A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580469 | |||||||
chr15:73580469 | TTATATAT others(9): Show |
T | 2 | a0001c0001t0001g0226 a0001c0001t0001g0228 |
2 | HG02615.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.707-6690_707-6675d others(18): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580469 | |||||||
chr15:73580478 | C | CAAA | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6684_707-6683i others(5): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580478 | |||||||
chr15:73580482 | A | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6687T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580482 | |||||||
chr15:73580482 | AAT | A | 5 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(2): Show |
5 | HG02559.hp1 HG02970.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.707-6689_707-6688d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580482 | |||||||
chr15:73580485 | A | T | 8 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(5): Show |
11 | HG01496.hp2 HG02055.hp2 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.707-6690T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580485 | |||||||
chr15:73580498 | AATAT | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0141 a0001c0001t0003g0040 others(2): Show |
6 | NA18952.hp1 NA18965.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.707-6707_707-6704d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580498 | |||||||
chr15:73580516 | A | AAT | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.707-6723_707-6722d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580516 | |||||||
chr15:73580516 | AAT | A | 14 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0046 others(11): Show |
17 | HG01496.hp2 HG02055.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.707-6723_707-6722d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580516 | |||||||
chr15:73580523 | TTATATAT others(20): Show |
T | 3 | a0001c0001t0001g0013 a0001c0001t0001g0059 a0001c0001t0001g0067 |
4 | NA18942.hp2 NA18952.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.707-6755_707-6729d others(29): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580523 | |||||||
chr15:73580569 | TTATATAT others(20): Show |
T | 23 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(20): Show |
23 | HG00438.hp1 HG00735.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.707-6801_707-6775d others(29): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580569 | |||||||
chr15:73580572 | T | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
7 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.707-6777A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580572 | |||||||
chr15:73580588 | TTATATAT others(1): Show |
T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.707-6801_707-6794d others(10): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580588 | |||||||
chr15:73580623 | G | GTATATAT others(12): Show |
1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.707-6847_707-6829d others(21): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580623 | |||||||
chr15:73580656 | ATT | A | 2 | a0001c0001t0001g0011 a0001c0001t0001g0184 |
4 | HG00597.hp1 HG02071.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.707-6863_707-6862d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580656 | |||||||
chr15:73580664 | C | A | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
122 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.706+6860G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580664 | |||||||
chr15:73580721 | T | A | 1 | a0001c0001t0001g0259 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.706+6803A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580721 | |||||||
chr15:73580798 | T | C | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.706+6726A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580798 | |||||||
chr15:73580828 | G | C | 1 | a0001c0001t0001g0149 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.706+6696C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580828 | |||||||
chr15:73580933 | T | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0110 |
2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.706+6591A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580933 | |||||||
chr15:73580952 | C | CT | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+6571dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73580952 | |||||||
chr15:73581067 | G | A | 4 | a0001c0001t0001g0019 a0001c0001t0001g0111 a0001c0001t0001g0115 others(1): Show |
5 | HG01361.hp1 HG01928.hp1 HG01952.hp2 others(2): Show |
intron_variant | MODIFIER | c.706+6457C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581067 | |||||||
chr15:73581124 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.706+6400G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581124 | |||||||
chr15:73581502 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.706+6022G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581502 | |||||||
chr15:73581540 | C | T | 5 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0154 others(2): Show |
5 | HG01943.hp2 HG01981.hp1 NA18942.hp1 others(2): Show |
intron_variant | MODIFIER | c.706+5984G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581540 | |||||||
chr15:73581605 | C | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
10 | HG00621.hp2 HG02132.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+5919G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581605 | |||||||
chr15:73581673 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.706+5851A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581673 | |||||||
chr15:73581703 | C | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.706+5821G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581703 | |||||||
chr15:73581757 | T | C | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.706+5767A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581757 | |||||||
chr15:73581826 | A | T | 1 | a0001c0001t0001g0255 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.706+5698T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581826 | |||||||
chr15:73581836 | C | CT | 6 | a0001c0001t0001g0016 a0001c0001t0001g0039 a0001c0001t0001g0255 others(3): Show |
8 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.706+5687dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581836 | |||||||
chr15:73581848 | C | T | 48 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
54 | HG00438.hp1 HG00558.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.706+5676G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581848 | |||||||
chr15:73581971 | A | G | 1 | a0001c0001t0001g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.706+5553T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73581971 | |||||||
chr15:73582020 | G | C | 1 | a0001c0001t0001g0039 | 2 | HG01243.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.706+5504C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582020 | |||||||
chr15:73582307 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.706+5217A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582307 | |||||||
chr15:73582400 | G | A | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.706+5124C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582400 | |||||||
chr15:73582573 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.706+4951G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582573 | |||||||
chr15:73582591 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+4933G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582591 | |||||||
chr15:73582868 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+4656G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582868 | |||||||
chr15:73582888 | T | C | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.706+4636A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582888 | |||||||
chr15:73582946 | C | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.706+4578G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73582946 | |||||||
chr15:73583272 | G | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.706+4252C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583272 | |||||||
chr15:73583326 | C | T | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.706+4198G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583326 | |||||||
chr15:73583385 | C | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.706+4139G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583385 | |||||||
chr15:73583487 | G | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+4037C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583487 | |||||||
chr15:73583881 | G | A | 49 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
55 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.706+3643C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73583881 | |||||||
chr15:73584068 | C | A | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.706+3456G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584068 | |||||||
chr15:73584081 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.706+3443G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584081 | |||||||
chr15:73584290 | T | G | 3 | a0001c0001t0003g0040 a0001c0001t0003g0041 a0001c0001t0003g0042 |
3 | NA18965.hp2 NA18994.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.706+3234A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584290 | |||||||
chr15:73584660 | C | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
107 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.706+2864G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584660 | |||||||
chr15:73584702 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.706+2822A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584702 | |||||||
chr15:73584764 | T | TA | 37 | a0001c0001t0001g0025 a0001c0001t0001g0034 a0001c0001t0001g0035 others(34): Show |
44 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(41): Show |
intron_variant | MODIFIER | c.706+2759dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584764 | |||||||
chr15:73584764 | TA | T | 10 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0099 others(7): Show |
10 | HG01069.hp2 HG01169.hp1 HG02155.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+2759delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584764 | |||||||
chr15:73584765 | A | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0063 others(2): Show |
6 | NA18969.hp2 NA18975.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.706+2759T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584765 | |||||||
chr15:73584806 | C | T | 1 | a0001c0001t0001g0018 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.706+2718G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584806 | |||||||
chr15:73584963 | T | C | 4 | a0001c0001t0001g0038 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
5 | HG02293.hp2 NA18974.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.706+2561A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73584963 | |||||||
chr15:73585039 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.706+2485G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585039 | |||||||
chr15:73585149 | T | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.706+2375A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585149 | |||||||
chr15:73585149 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.706+2375A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585149 | |||||||
chr15:73585419 | A | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+2105T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585419 | |||||||
chr15:73585435 | G | A | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.706+2089C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585435 | |||||||
chr15:73585678 | A | G | 96 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(93): Show |
120 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.706+1846T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585678 | |||||||
chr15:73585768 | C | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0092 |
2 | HG00544.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.706+1756G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585768 | |||||||
chr15:73585886 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0148 |
2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.706+1638C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585886 | |||||||
chr15:73585888 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.706+1636C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585888 | |||||||
chr15:73585934 | A | G | 1 | a0001c0001t0001g0021 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.706+1590T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585934 | |||||||
chr15:73585969 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.706+1555G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585969 | |||||||
chr15:73585986 | G | A | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.706+1538C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73585986 | |||||||
chr15:73586203 | G | A | 1 | a0001c0001t0002g0220 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.706+1321C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586203 | |||||||
chr15:73586229 | A | G | 176 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(173): Show |
217 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(214): Show |
intron_variant | MODIFIER | c.706+1295T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586229 | |||||||
chr15:73586491 | A | C | 1 | a0001c0001t0001g0121 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.706+1033T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586491 | |||||||
chr15:73586802 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.706+722A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73586802 | |||||||
chr15:73587151 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.706+373G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587151 | |||||||
chr15:73587155 | G | C | 1 | a0001c0001t0001g0116 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.706+369C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587155 | |||||||
chr15:73587251 | C | A | 8 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0078 others(5): Show |
10 | HG00621.hp2 HG02132.hp1 NA18950.hp2 others(7): Show |
intron_variant | MODIFIER | c.706+273G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587251 | |||||||
chr15:73587299 | G | A | 1 | a0001c0001t0001g0241 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.706+225C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 4/8 | chr15 | 73587299 | |||||||
chr15:73587692 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-74C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587692 | |||||||
chr15:73587729 | C | A | 1 | a0001c0001t0001g0089 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.612-111G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587729 | |||||||
chr15:73587752 | A | G | 1 | a0001c0001t0001g0136 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.612-134T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587752 | |||||||
chr15:73587926 | G | A | 4 | a0001c0001t0001g0038 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
5 | HG02293.hp2 NA18974.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-308C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587926 | |||||||
chr15:73587977 | C | G | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.612-359G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587977 | |||||||
chr15:73587982 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.612-364G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73587982 | |||||||
chr15:73588414 | G | A | 6 | a0001c0001t0001g0135 a0001c0001t0001g0136 a0001c0001t0001g0137 others(3): Show |
6 | HG02523.hp2 NA18998.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.612-796C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588414 | |||||||
chr15:73588439 | G | T | 10 | a0001c0001t0001g0005 a0001c0001t0001g0224 a0001c0001t0001g0225 others(7): Show |
13 | HG01496.hp2 HG02055.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.612-821C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588439 | |||||||
chr15:73588502 | C | A | 1 | a0001c0001t0001g0260 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-884G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588502 | |||||||
chr15:73588503 | A | G | 1 | a0001c0001t0001g0260 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-885T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588503 | |||||||
chr15:73588506 | G | C | 1 | a0001c0001t0001g0260 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.612-888C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588506 | |||||||
chr15:73588986 | A | T | 1 | a0001c0001t0001g0021 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.612-1368T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73588986 | |||||||
chr15:73589083 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-1465C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589083 | |||||||
chr15:73589254 | C | T | 1 | a0001c0001t0001g0167 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.612-1636G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589254 | |||||||
chr15:73589396 | C | T | 4 | a0001c0001t0001g0038 a0001c0001t0001g0264 a0001c0001t0001g0265 others(1): Show |
5 | HG02293.hp2 NA18974.hp1 NA19054.hp2 others(2): Show |
intron_variant | MODIFIER | c.612-1778G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589396 | |||||||
chr15:73589427 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-1809G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589427 | |||||||
chr15:73589504 | A | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 |
5 | HG02145.hp1 HG02622.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-1886T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589504 | |||||||
chr15:73589592 | G | T | 1 | a0001c0001t0001g0196 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.612-1974C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589592 | |||||||
chr15:73589715 | G | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-2097C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589715 | |||||||
chr15:73589753 | T | C | 5 | a0001c0001t0001g0253 a0001c0001t0001g0255 a0001c0001t0001g0256 others(2): Show |
5 | NA18949.hp2 NA18961.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-2135A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589753 | |||||||
chr15:73589817 | C | CAA | 270 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(267): Show |
329 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(326): Show |
intron_variant | MODIFIER | c.611+2148_611+2149i others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73589817 | |||||||
chr15:73590126 | T | C | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.611+1840A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590126 | |||||||
chr15:73590416 | A | G | 1 | a0001c0001t0001g0102 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.611+1550T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590416 | |||||||
chr15:73590607 | C | CA | 68 | a0001c0001t0001g0010 a0001c0001t0001g0034 a0001c0001t0001g0035 others(65): Show |
80 | HG00438.hp1 HG00558.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.611+1358dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590607 | |||||||
chr15:73590884 | T | A | 1 | a0001c0001t0001g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.611+1082A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590884 | |||||||
chr15:73590884 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.611+1082A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590884 | |||||||
chr15:73590923 | G | A | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.611+1043C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73590923 | |||||||
chr15:73591198 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.611+768C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591198 | |||||||
chr15:73591519 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.611+447G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591519 | |||||||
chr15:73591582 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+384A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591582 | |||||||
chr15:73591751 | A | G | 6 | a0001c0001t0001g0142 a0001c0001t0001g0152 a0001c0001t0001g0154 others(3): Show |
6 | HG01943.hp2 HG01952.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.611+215T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591751 | |||||||
chr15:73591826 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+140C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591826 | |||||||
chr15:73591941 | C | T | 1 | a0001c0001t0001g0033 | 2 | HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.611+25G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 3/8 | chr15 | 73591941 | |||||||
chr15:73592184 | C | T | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.440-47G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592184 | |||||||
chr15:73592367 | C | T | 44 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(41): Show |
50 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.440-230G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592367 | |||||||
chr15:73592447 | C | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0204 |
2 | HG01261.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.440-310G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592447 | |||||||
chr15:73592470 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.440-333A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592470 | |||||||
chr15:73592560 | C | A | 5 | a0001c0001t0001g0026 a0001c0001t0001g0141 a0001c0001t0003g0040 others(2): Show |
6 | NA18952.hp1 NA18965.hp2 NA18986.hp2 others(3): Show |
intron_variant | MODIFIER | c.440-423G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592560 | |||||||
chr15:73592625 | G | A | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG00438.hp1 HG02155.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-488C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592625 | |||||||
chr15:73592627 | C | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.440-490G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592627 | |||||||
chr15:73592806 | C | T | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.440-669G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73592806 | |||||||
chr15:73593062 | G | A | 2 | a0001c0001t0001g0044 a0001c0001t0006g0279 |
2 | HG01346.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.440-925C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593062 | |||||||
chr15:73593102 | G | A | 44 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(41): Show |
50 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.440-965C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593102 | |||||||
chr15:73593198 | T | C | 98 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(95): Show |
122 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.440-1061A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593198 | |||||||
chr15:73593303 | A | G | 5 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
7 | HG01346.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-1166T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593303 | |||||||
chr15:73593504 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
7 | HG01346.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-1367G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593504 | |||||||
chr15:73593927 | G | A | 1 | a0001c0001t0001g0124 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.440-1790C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593927 | |||||||
chr15:73593956 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.440-1819C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73593956 | |||||||
chr15:73594085 | A | G | 1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.440-1948T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594085 | |||||||
chr15:73594508 | G | T | 84 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(81): Show |
107 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(104): Show |
intron_variant | MODIFIER | c.440-2371C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594508 | |||||||
chr15:73594534 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.440-2397G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594534 | |||||||
chr15:73594871 | C | A | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | HG00673.hp2 NA18955.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2151G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594871 | |||||||
chr15:73594951 | T | A | 4 | a0001c0001t0001g0086 a0001c0001t0001g0092 a0001c0001t0001g0161 others(1): Show |
4 | HG00544.hp1 NA18949.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.439+2071A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594951 | |||||||
chr15:73594951 | T | TA | 34 | a0001c0001t0001g0010 a0001c0001t0001g0118 a0001c0001t0001g0128 others(31): Show |
39 | HG00438.hp1 HG01109.hp1 HG01346.hp1 others(36): Show |
intron_variant | MODIFIER | c.439+2070dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594951 | |||||||
chr15:73594951 | TA | T | 9 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(6): Show |
9 | HG02559.hp1 HG02897.hp2 NA18522.hp2 others(6): Show |
intron_variant | MODIFIER | c.439+2070delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73594951 | |||||||
chr15:73595005 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.439+2017T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595005 | |||||||
chr15:73595116 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.439+1906A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595116 | |||||||
chr15:73595143 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.439+1879G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595143 | |||||||
chr15:73595345 | T | TA | 13 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0118 others(10): Show |
14 | HG01109.hp1 HG01243.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.439+1676dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595345 | |||||||
chr15:73595384 | A | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.439+1638T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595384 | |||||||
chr15:73595564 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.439+1458C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595564 | |||||||
chr15:73595642 | A | G | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.439+1380T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595642 | |||||||
chr15:73595750 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.439+1272G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595750 | |||||||
chr15:73595824 | T | C | 1 | a0001c0001t0001g0106 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.439+1198A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595824 | |||||||
chr15:73595838 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.439+1184A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595838 | |||||||
chr15:73595890 | CAT | C | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.439+1130_439+1131d others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595890 | |||||||
chr15:73595896 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0090 a0001c0001t0001g0091 others(1): Show |
5 | NA18962.hp1 NA18968.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+1126A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595896 | |||||||
chr15:73595981 | G | C | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.439+1041C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73595981 | |||||||
chr15:73596574 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.439+448G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73596574 | |||||||
chr15:73596748 | G | A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.439+274C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 2/8 | chr15 | 73596748 | |||||||
chr15:73597386 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.92-17G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597386 | |||||||
chr15:73597411 | G | GA | 9 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.92-43dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597411 | |||||||
chr15:73597690 | C | T | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.92-321G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597690 | |||||||
chr15:73597785 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.92-416A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597785 | |||||||
chr15:73597829 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-460G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73597829 | |||||||
chr15:73598041 | C | G | 53 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(50): Show |
62 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.92-672G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598041 | |||||||
chr15:73598202 | A | G | 1 | a0001c0001t0001g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.92-833T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598202 | |||||||
chr15:73598273 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.92-904A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598273 | |||||||
chr15:73598284 | C | T | 1 | a0001c0001t0001g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.92-915G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598284 | |||||||
chr15:73598302 | G | C | 1 | a0001c0001t0001g0257 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.92-933C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598302 | |||||||
chr15:73598302 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.92-933C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598302 | |||||||
chr15:73598472 | T | TA | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-1104dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598472 | |||||||
chr15:73598472 | TA | T | 11 | a0001c0001t0001g0132 a0001c0001t0001g0165 a0001c0001t0001g0191 others(8): Show |
11 | HG00621.hp1 HG00673.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-1104delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598472 | |||||||
chr15:73598695 | A | G | 1 | a0001c0001t0001g0164 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.92-1326T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598695 | |||||||
chr15:73598939 | T | C | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-1570A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73598939 | |||||||
chr15:73599192 | G | GAGCCCCC others(1): Show |
6 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(3): Show |
7 | HG01243.hp2 HG01255.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-1831_92-1824dup others(8): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599192 | |||||||
chr15:73599388 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-2019C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599388 | |||||||
chr15:73599449 | A | G | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.92-2080T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599449 | |||||||
chr15:73599507 | G | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.92-2138C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599507 | |||||||
chr15:73599648 | A | AAGGG | 42 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(39): Show |
48 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.92-2283_92-2280dup others(4): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599648 | |||||||
chr15:73599854 | C | T | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-2485G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73599854 | |||||||
chr15:73600037 | T | C | 53 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(50): Show |
62 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.92-2668A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600037 | |||||||
chr15:73600095 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.92-2726A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600095 | |||||||
chr15:73600129 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.92-2760T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600129 | |||||||
chr15:73600130 | G | T | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.92-2761C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600130 | |||||||
chr15:73600325 | G | GACATTTT others(9): Show |
71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
85 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.92-2957_92-2956ins others(16): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600325 | |||||||
chr15:73600348 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92-2979A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600348 | |||||||
chr15:73600349 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.92-2980A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600349 | |||||||
chr15:73600611 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
209 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.92-3242A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600611 | |||||||
chr15:73600647 | T | C | 1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-3278A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600647 | |||||||
chr15:73600882 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.92-3513G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600882 | |||||||
chr15:73600940 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3571C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600940 | |||||||
chr15:73600951 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3582C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73600951 | |||||||
chr15:73601045 | C | T | 2 | a0001c0001t0001g0039 a0001c0001t0001g0277 |
3 | HG01243.hp2 HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.92-3676G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601045 | |||||||
chr15:73601046 | G | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-3677C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601046 | |||||||
chr15:73601278 | C | T | 10 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(7): Show |
10 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.92-3909G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601278 | |||||||
chr15:73601283 | CA | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-3915delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601283 | |||||||
chr15:73601907 | C | T | 3 | a0001c0001t0001g0039 a0001c0001t0001g0277 a0001c0001t0001g0278 |
4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-4538G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601907 | |||||||
chr15:73601935 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-4566C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73601935 | |||||||
chr15:73602179 | AC | A | 273 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(270): Show |
332 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(329): Show |
intron_variant | MODIFIER | c.92-4811delG | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602179 | |||||||
chr15:73602377 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-5008G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602377 | |||||||
chr15:73602482 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.92-5113C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602482 | |||||||
chr15:73602639 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.92-5270C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602639 | |||||||
chr15:73602833 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.92-5464G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602833 | |||||||
chr15:73602934 | C | A | 1 | a0001c0001t0001g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.92-5565G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602934 | |||||||
chr15:73602952 | G | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-5583C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602952 | |||||||
chr15:73602969 | C | G | 1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-5600G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602969 | |||||||
chr15:73602989 | G | C | 25 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(22): Show |
30 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.92-5620C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602989 | |||||||
chr15:73602991 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.92-5622C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73602991 | |||||||
chr15:73603266 | T | C | 12 | a0001c0001t0001g0215 a0001c0001t0002g0012 a0001c0001t0002g0030 others(9): Show |
17 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-5897A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603266 | |||||||
chr15:73603314 | G | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-5945C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603314 | |||||||
chr15:73603485 | A | G | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-6116T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603485 | |||||||
chr15:73603510 | T | C | 169 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(166): Show |
207 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(204): Show |
intron_variant | MODIFIER | c.92-6141A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603510 | |||||||
chr15:73603511 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.92-6142C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603511 | |||||||
chr15:73603574 | CAG | C | 12 | a0001c0001t0001g0215 a0001c0001t0002g0012 a0001c0001t0002g0030 others(9): Show |
17 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-6207_92-6206del others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603574 | |||||||
chr15:73603752 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.92-6383A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73603752 | |||||||
chr15:73604011 | G | C | 1 | a0001c0001t0002g0222 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.92-6642C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604011 | |||||||
chr15:73604027 | G | A | 3 | a0001c0001t0001g0009 a0001c0001t0001g0112 a0001c0001t0001g0117 |
5 | HG00280.hp1 HG00642.hp1 HG00738.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-6658C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604027 | |||||||
chr15:73604079 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-6710G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604079 | |||||||
chr15:73604247 | C | T | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
216 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.92-6878G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604247 | |||||||
chr15:73604268 | G | A | 1 | a0001c0001t0001g0258 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.92-6899C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604268 | |||||||
chr15:73604328 | A | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
85 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.92-6959T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604328 | |||||||
chr15:73604554 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.92-7185A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604554 | |||||||
chr15:73604667 | A | G | 11 | a0001c0001t0001g0215 a0001c0001t0002g0012 a0001c0001t0002g0030 others(8): Show |
16 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.92-7298T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73604667 | |||||||
chr15:73605067 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.92-7698G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605067 | |||||||
chr15:73605099 | A | AG | 18 | a0001c0001t0001g0023 a0001c0001t0001g0024 a0001c0001t0001g0035 others(15): Show |
22 | HG00621.hp1 HG01109.hp2 HG01261.hp2 others(19): Show |
intron_variant | MODIFIER | c.92-7731dupC | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605099 | |||||||
chr15:73605099 | A | AGGCGGGG others(5): Show |
1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-7731_92-7730ins others(12): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605099 | |||||||
chr15:73605099 | A | AGGGGGGG others(4): Show |
1 | a0001c0002t0001g0273 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.92-7741_92-7731dup others(11): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605099 | |||||||
chr15:73605102 | G | C | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-7733C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605102 | |||||||
chr15:73605104 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.92-7735C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605104 | |||||||
chr15:73605104 | G | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0057 |
5 | HG01891.hp1 NA18948.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.92-7735C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605104 | |||||||
chr15:73605104 | G | T | 5 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0144 others(2): Show |
8 | HG00558.hp2 HG00597.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.92-7735C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605104 | |||||||
chr15:73605110 | G | GA | 13 | a0001c0001t0001g0005 a0001c0001t0001g0215 a0001c0001t0001g0230 others(10): Show |
20 | HG01496.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-7742_92-7741ins others(1): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605110 | |||||||
chr15:73605111 | G | A | 125 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(122): Show |
161 | HG00280.hp1 HG00280.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.92-7742C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | |||||||
chr15:73605111 | G | GA | 11 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0069 others(8): Show |
12 | HG00597.hp2 HG01261.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.92-7743dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | |||||||
chr15:73605111 | G | GAA | 4 | a0001c0001t0001g0227 a0001c0001t0001g0228 a0001c0001t0001g0263 others(1): Show |
4 | HG02071.hp2 HG02809.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-7744_92-7743dup others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | |||||||
chr15:73605111 | GAA | G | 3 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 |
4 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-7744_92-7743del others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605111 | |||||||
chr15:73605112 | A | G | 53 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(50): Show |
58 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.92-7743T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605112 | |||||||
chr15:73605113 | A | G | 18 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
18 | HG00438.hp1 HG02155.hp2 HG02280.hp1 others(15): Show |
intron_variant | MODIFIER | c.92-7744T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605113 | |||||||
chr15:73605114 | A | G | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-7745T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605114 | |||||||
chr15:73605170 | G | A | 1 | a0001c0001t0001g0092 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.92-7801C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605170 | |||||||
chr15:73605299 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.92-7930A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605299 | |||||||
chr15:73605330 | T | C | 21 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(18): Show |
25 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.92-7961A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605330 | |||||||
chr15:73605376 | T | TA | 9 | a0001c0001t0001g0008 a0001c0001t0001g0077 a0001c0001t0001g0078 others(6): Show |
11 | HG00621.hp2 HG02132.hp1 HG03209.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-8008dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605376 | |||||||
chr15:73605394 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0080 others(1): Show |
4 | NA18950.hp2 NA19063.hp1 NA19078.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-8025G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605394 | |||||||
chr15:73605435 | T | C | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.92-8066A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605435 | |||||||
chr15:73605454 | T | C | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-8085A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605454 | |||||||
chr15:73605510 | C | A | 2 | a0001c0001t0001g0201 a0001c0001t0001g0206 |
2 | HG03239.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.92-8141G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605510 | |||||||
chr15:73605623 | G | A | 12 | a0001c0001t0001g0215 a0001c0001t0002g0012 a0001c0001t0002g0030 others(9): Show |
17 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.92-8254C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605623 | |||||||
chr15:73605658 | G | GC | 48 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(45): Show |
54 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.92-8290_92-8289ins others(1): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605658 | |||||||
chr15:73605726 | CA | C | 87 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(84): Show |
110 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.92-8358delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605726 | |||||||
chr15:73605846 | A | G | 1 | a0001c0001t0001g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.92-8477T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73605846 | |||||||
chr15:73606054 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.92-8685T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606054 | |||||||
chr15:73606373 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.92-9004T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606373 | |||||||
chr15:73606467 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.92-9098A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606467 | |||||||
chr15:73606520 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-9151A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606520 | |||||||
chr15:73606701 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-9332C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606701 | |||||||
chr15:73606851 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.92-9482G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606851 | |||||||
chr15:73606939 | CAG | C | 6 | a0001c0001t0001g0020 a0001c0001t0001g0050 a0001c0001t0001g0119 others(3): Show |
7 | HG01243.hp1 HG02109.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-9572_92-9571del others(2): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73606939 | |||||||
chr15:73607047 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-9678G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607047 | |||||||
chr15:73607339 | G | A | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.92-9970C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607339 | |||||||
chr15:73607360 | A | C | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG00438.hp1 HG02155.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-9991T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607360 | |||||||
chr15:73607411 | C | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
85 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.92-10042G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607411 | |||||||
chr15:73607467 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.92-10098G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607467 | |||||||
chr15:73607524 | G | A | 3 | a0001c0001t0001g0028 a0001c0001t0001g0145 a0001c0001t0001g0175 |
4 | HG02300.hp1 NA18960.hp1 NA18971.hp1 others(1): Show |
intron_variant | MODIFIER | c.92-10155C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607524 | |||||||
chr15:73607694 | T | C | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.92-10325A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607694 | |||||||
chr15:73607721 | A | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-10352T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607721 | |||||||
chr15:73607818 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-10449C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607818 | |||||||
chr15:73607830 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.92-10461G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607830 | |||||||
chr15:73607878 | G | A | 1 | a0001c0001t0003g0042 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.92-10509C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607878 | |||||||
chr15:73607951 | T | C | 2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.92-10582A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607951 | |||||||
chr15:73607966 | T | C | 5 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
7 | HG01346.hp1 HG02145.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-10597A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73607966 | |||||||
chr15:73608022 | T | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
85 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.92-10653A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608022 | |||||||
chr15:73608063 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.92-10694A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608063 | |||||||
chr15:73608071 | C | A | 1 | a0001c0001t0001g0018 | 2 | HG02735.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.92-10702G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608071 | |||||||
chr15:73608382 | T | C | 1 | a0001c0001t0001g0176 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.92-11013A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608382 | |||||||
chr15:73608511 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.92-11142A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608511 | |||||||
chr15:73608629 | A | ATTCTAAA others(9): Show |
71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
85 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.92-11261_92-11260i others(18): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608629 | |||||||
chr15:73608666 | TCTGA | T | 7 | a0001c0001t0001g0038 a0001c0001t0001g0248 a0001c0001t0001g0250 others(4): Show |
8 | HG02015.hp2 HG02083.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.92-11301_92-11298d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608666 | |||||||
chr15:73608822 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.92-11453T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608822 | |||||||
chr15:73608854 | C | T | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.92-11485G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73608854 | |||||||
chr15:73609005 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.92-11636C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609005 | |||||||
chr15:73609201 | ATATTT | A | 5 | a0001c0001t0001g0015 a0001c0001t0001g0058 a0001c0001t0001g0063 others(2): Show |
6 | NA18969.hp2 NA18975.hp1 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-11837_92-11833d others(7): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609201 | |||||||
chr15:73609317 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0124 |
3 | HG01261.hp1 HG01496.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.92-11948C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609317 | |||||||
chr15:73609409 | TCACCTGA others(5): Show |
T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-12052_92-12041d others(14): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609409 | |||||||
chr15:73609472 | A | G | 1 | a0001c0001t0005g0261 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.92-12103T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609472 | |||||||
chr15:73609633 | A | AAAAC | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-12268_92-12265d others(6): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609633 | |||||||
chr15:73609798 | T | C | 2 | a0001c0001t0001g0039 a0001c0001t0001g0277 |
3 | HG01243.hp2 HG01255.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.92-12429A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609798 | |||||||
chr15:73609948 | T | A | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-12579A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73609948 | |||||||
chr15:73610005 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.92-12636G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610005 | |||||||
chr15:73610090 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.92-12721A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610090 | |||||||
chr15:73610093 | T | C | 11 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(8): Show |
11 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.92-12724A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610093 | |||||||
chr15:73610770 | C | A | 1 | a0001c0001t0001g0190 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.92-13401G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73610770 | |||||||
chr15:73611045 | T | A | 1 | a0001c0001t0001g0211 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.92-13676A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611045 | |||||||
chr15:73611238 | T | G | 1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.92-13869A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611238 | |||||||
chr15:73611320 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.92-13951A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611320 | |||||||
chr15:73611554 | T | C | 1 | a0001c0001t0001g0178 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.92-14185A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611554 | |||||||
chr15:73611649 | T | A | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-14280A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611649 | |||||||
chr15:73611680 | T | C | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.92-14311A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611680 | |||||||
chr15:73611726 | C | T | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-14357G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611726 | |||||||
chr15:73611749 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-14380C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611749 | |||||||
chr15:73611943 | G | A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.92-14574C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73611943 | |||||||
chr15:73612151 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.92-14782A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612151 | |||||||
chr15:73612409 | G | T | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-15040C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612409 | |||||||
chr15:73612420 | CA | C | 172 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(169): Show |
213 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(210): Show |
intron_variant | MODIFIER | c.92-15052delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612420 | |||||||
chr15:73612441 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.92-15072T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612441 | |||||||
chr15:73612494 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.92-15125C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612494 | |||||||
chr15:73612533 | C | T | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.92-15164G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612533 | |||||||
chr15:73612583 | T | C | 170 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(167): Show |
209 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(206): Show |
intron_variant | MODIFIER | c.92-15214A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612583 | |||||||
chr15:73612901 | C | T | 1 | a0001c0001t0003g0040 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.92-15532G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73612901 | |||||||
chr15:73613411 | A | G | 7 | a0001c0001t0001g0043 a0001c0001t0001g0106 a0001c0001t0001g0107 others(4): Show |
7 | HG01192.hp2 HG01258.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.92-16042T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613411 | |||||||
chr15:73613664 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-16295C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613664 | |||||||
chr15:73613671 | G | A | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.92-16302C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613671 | |||||||
chr15:73613716 | C | T | 1 | a0001c0001t0001g0201 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.92-16347G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613716 | |||||||
chr15:73613977 | T | G | 1 | a0001c0001t0001g0245 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.92-16608A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73613977 | |||||||
chr15:73614081 | G | A | 1 | a0001c0001t0001g0021 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.92-16712C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614081 | |||||||
chr15:73614157 | C | CA | 12 | a0001c0001t0001g0039 a0001c0001t0001g0179 a0001c0001t0001g0180 others(9): Show |
13 | HG00673.hp1 HG01243.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.92-16789dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614157 | |||||||
chr15:73614173 | A | T | 1 | a0001c0001t0001g0128 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.92-16804T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614173 | |||||||
chr15:73614319 | T | TA | 110 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(107): Show |
139 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(136): Show |
intron_variant | MODIFIER | c.92-16951dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614319 | |||||||
chr15:73614319 | TA | T | 11 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG02055.hp2 HG02559.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.92-16951delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614319 | |||||||
chr15:73614366 | A | G | 57 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(54): Show |
77 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.92-16997T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614366 | |||||||
chr15:73614544 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.92-17175T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614544 | |||||||
chr15:73614687 | T | C | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-17318A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614687 | |||||||
chr15:73614698 | GA | G | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.92-17330delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614698 | |||||||
chr15:73614772 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.92-17403T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73614772 | |||||||
chr15:73615025 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.92-17656A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615025 | |||||||
chr15:73615098 | G | C | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-17729C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615098 | |||||||
chr15:73615100 | T | TGGA | 3 | a0001c0001t0001g0007 a0001c0001t0001g0057 a0001c0001t0001g0104 |
5 | NA18948.hp1 NA18964.hp2 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.92-17734_92-17732d others(5): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615100 | |||||||
chr15:73615104 | T | A | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.92-17735A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615104 | |||||||
chr15:73615156 | C | CT | 15 | a0001c0001t0001g0058 a0001c0001t0001g0101 a0001c0001t0001g0102 others(12): Show |
20 | HG00673.hp2 HG01516.hp1 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.92-17788dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615156 | |||||||
chr15:73615156 | CT | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
80 | HG00438.hp1 HG00639.hp1 HG01074.hp2 others(77): Show |
intron_variant | MODIFIER | c.92-17788delA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615156 | |||||||
chr15:73615173 | T | A | 1 | a0001c0001t0001g0259 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.92-17804A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615173 | |||||||
chr15:73615174 | A | T | 2 | a0001c0001t0001g0054 a0001c0001t0001g0057 |
2 | HG00639.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.92-17805T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615174 | |||||||
chr15:73615315 | A | G | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+17810T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615315 | |||||||
chr15:73615350 | A | T | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.91+17775T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615350 | |||||||
chr15:73615663 | T | G | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+17462A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615663 | |||||||
chr15:73615824 | T | C | 1 | a0001c0001t0001g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.91+17301A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615824 | |||||||
chr15:73615871 | A | G | 49 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(46): Show |
55 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.91+17254T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615871 | |||||||
chr15:73615980 | A | G | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+17145T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73615980 | |||||||
chr15:73616038 | A | AT | 3 | a0001c0001t0001g0010 a0001c0001t0001g0138 a0001c0001t0001g0139 |
5 | HG02145.hp1 HG02622.hp2 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+17086dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616038 | |||||||
chr15:73616407 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.91+16718C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616407 | |||||||
chr15:73616447 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+16678G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616447 | |||||||
chr15:73616462 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.91+16663C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616462 | |||||||
chr15:73616529 | C | T | 1 | a0001c0001t0001g0056 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.91+16596G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616529 | |||||||
chr15:73616534 | G | A | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+16591C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616534 | |||||||
chr15:73616579 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.91+16546G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616579 | |||||||
chr15:73616593 | A | C | 1 | a0001c0001t0001g0143 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.91+16532T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616593 | |||||||
chr15:73616618 | C | T | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+16507G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616618 | |||||||
chr15:73616676 | C | G | 1 | a0001c0001t0001g0016 | 2 | NA18968.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.91+16449G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73616676 | |||||||
chr15:73617456 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.91+15669A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73617456 | |||||||
chr15:73617466 | T | G | 28 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(25): Show |
33 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(30): Show |
intron_variant | MODIFIER | c.91+15659A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73617466 | |||||||
chr15:73617949 | A | G | 12 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(9): Show |
12 | HG00438.hp1 HG01891.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.91+15176T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73617949 | |||||||
chr15:73618033 | A | G | 171 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(168): Show |
210 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(207): Show |
intron_variant | MODIFIER | c.91+15092T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618033 | |||||||
chr15:73618048 | G | A | 3 | a0001c0001t0001g0049 a0001c0001t0001g0189 a0001c0001t0001g0190 |
3 | HG00280.hp2 HG01081.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.91+15077C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618048 | |||||||
chr15:73618158 | C | A | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+14967G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618158 | |||||||
chr15:73618174 | A | C | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+14951T>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618174 | |||||||
chr15:73618467 | A | T | 1 | a0001c0001t0001g0236 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.91+14658T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618467 | |||||||
chr15:73618506 | T | C | 1 | a0001c0001t0001g0191 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.91+14619A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618506 | |||||||
chr15:73618703 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.91+14422C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618703 | |||||||
chr15:73618959 | T | C | 2 | a0001c0001t0001g0192 a0001c0001t0001g0193 |
2 | HG00673.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.91+14166A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618959 | |||||||
chr15:73618962 | G | C | 1 | a0001c0001t0001g0140 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.91+14163C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618962 | |||||||
chr15:73618991 | C | T | 1 | a0001c0001t0001g0224 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.91+14134G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73618991 | |||||||
chr15:73619062 | C | CA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0068 a0001c0001t0001g0128 others(21): Show |
31 | HG01496.hp2 HG01952.hp1 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.91+14062dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619062 | |||||||
chr15:73619062 | CA | C | 19 | a0001c0001t0001g0010 a0001c0001t0001g0079 a0001c0001t0001g0138 others(16): Show |
21 | HG00438.hp1 HG01346.hp1 HG01943.hp2 others(18): Show |
intron_variant | MODIFIER | c.91+14062delT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619062 | |||||||
chr15:73619456 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.91+13669T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619456 | |||||||
chr15:73619808 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.91+13317G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619808 | |||||||
chr15:73619979 | G | A | 4 | a0001c0001t0001g0005 a0001c0001t0001g0230 a0001c0001t0001g0231 others(1): Show |
7 | HG01496.hp2 HG02622.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.91+13146C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73619979 | |||||||
chr15:73620033 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+13092A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620033 | |||||||
chr15:73620165 | G | A | 1 | a0001c0001t0001g0069 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.91+12960C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620165 | |||||||
chr15:73620272 | C | T | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+12853G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620272 | |||||||
chr15:73620403 | A | G | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+12722T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620403 | |||||||
chr15:73620655 | T | C | 1 | a0001c0001t0001g0215 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.91+12470A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620655 | |||||||
chr15:73620817 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.91+12308A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620817 | |||||||
chr15:73620854 | G | GT | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+12270dupA | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620854 | |||||||
chr15:73620897 | C | G | 175 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0005 others(172): Show |
216 | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(213): Show |
intron_variant | MODIFIER | c.91+12228G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73620897 | |||||||
chr15:73621099 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.91+12026A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621099 | |||||||
chr15:73621231 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | NA19005.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.91+11894G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621231 | |||||||
chr15:73621332 | T | C | 1 | a0001c0001t0001g0071 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.91+11793A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621332 | |||||||
chr15:73621497 | A | G | 1 | a0001c0001t0001g0055 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.91+11628T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621497 | |||||||
chr15:73621681 | C | A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+11444G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621681 | |||||||
chr15:73621748 | C | T | 21 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0037 others(18): Show |
25 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.91+11377G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621748 | |||||||
chr15:73621778 | C | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+11347G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621778 | |||||||
chr15:73621914 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+11211T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73621914 | |||||||
chr15:73622022 | G | T | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+11103C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622022 | |||||||
chr15:73622048 | G | A | 1 | a0001c0001t0001g0029 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.91+11077C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622048 | |||||||
chr15:73622114 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.91+11011T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622114 | |||||||
chr15:73622170 | C | A | 1 | a0001c0001t0001g0198 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.91+10955G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622170 | |||||||
chr15:73622423 | A | T | 1 | a0001c0001t0001g0134 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.91+10702T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622423 | |||||||
chr15:73622451 | A | T | 1 | a0001c0001t0001g0248 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.91+10674T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622451 | |||||||
chr15:73622499 | T | A | 12 | a0001c0001t0001g0038 a0001c0001t0001g0224 a0001c0001t0001g0225 others(9): Show |
13 | HG02055.hp2 HG02293.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.91+10626A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622499 | |||||||
chr15:73622625 | T | C | 4 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(1): Show |
4 | HG00673.hp2 NA18955.hp1 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.91+10500A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622625 | |||||||
chr15:73622725 | T | C | 1 | a0001c0001t0001g0199 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.91+10400A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622725 | |||||||
chr15:73622777 | C | G | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+10348G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622777 | |||||||
chr15:73622886 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+10239C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622886 | |||||||
chr15:73622891 | T | A | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+10234A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622891 | |||||||
chr15:73622901 | T | G | 1 | a0001c0001t0001g0200 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.91+10224A>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622901 | |||||||
chr15:73622913 | C | T | 97 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(94): Show |
121 | HG00280.hp1 HG00544.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.91+10212G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73622913 | |||||||
chr15:73623115 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+10010G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623115 | |||||||
chr15:73623123 | A | G | 7 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(4): Show |
7 | HG00438.hp1 HG02155.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.91+10002T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623123 | |||||||
chr15:73623138 | T | A | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+9987A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623138 | |||||||
chr15:73623453 | C | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+9672G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623453 | |||||||
chr15:73623479 | G | A | 8 | a0001c0001t0001g0051 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG01261.hp2 HG01975.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.91+9646C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623479 | |||||||
chr15:73623696 | C | T | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+9429G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623696 | |||||||
chr15:73623796 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91+9329A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623796 | |||||||
chr15:73623811 | A | T | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+9314T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623811 | |||||||
chr15:73623849 | CCTA | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+9273_91+9275del others(3): Show |
NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623849 | |||||||
chr15:73623896 | C | T | 1 | a0001c0001t0002g0218 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.91+9229G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623896 | |||||||
chr15:73623979 | T | C | 1 | a0001c0001t0001g0229 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.91+9146A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73623979 | |||||||
chr15:73624042 | A | G | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+9083T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624042 | |||||||
chr15:73624161 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.91+8964C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624161 | |||||||
chr15:73624336 | T | A | 1 | a0001c0001t0001g0072 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.91+8789A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624336 | |||||||
chr15:73624638 | T | TA | 34 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(31): Show |
40 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(37): Show |
intron_variant | MODIFIER | c.91+8486dupT | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624638 | |||||||
chr15:73624648 | C | T | 61 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(58): Show |
81 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(78): Show |
intron_variant | MODIFIER | c.91+8477G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624648 | |||||||
chr15:73624834 | A | G | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+8291T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624834 | |||||||
chr15:73624946 | C | A | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+8179G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73624946 | |||||||
chr15:73625009 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.91+8116T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625009 | |||||||
chr15:73625035 | T | C | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+8090A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625035 | |||||||
chr15:73625133 | C | T | 2 | a0001c0001t0001g0077 a0001c0001t0001g0078 |
2 | NA19063.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.91+7992G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625133 | |||||||
chr15:73625353 | A | G | 1 | a0001c0001t0001g0076 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.91+7772T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625353 | |||||||
chr15:73625378 | T | C | 25 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(22): Show |
30 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.91+7747A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625378 | |||||||
chr15:73625428 | G | A | 1 | a0001c0001t0001g0272 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.91+7697C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625428 | |||||||
chr15:73625506 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.91+7619A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625506 | |||||||
chr15:73625521 | T | C | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+7604A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625521 | |||||||
chr15:73625567 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+7558C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625567 | |||||||
chr15:73625633 | G | C | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(23): Show |
31 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(28): Show |
intron_variant | MODIFIER | c.91+7492C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625633 | |||||||
chr15:73625685 | T | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+7440A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625685 | |||||||
chr15:73625972 | A | G | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+7153T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73625972 | |||||||
chr15:73626147 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.91+6978C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626147 | |||||||
chr15:73626157 | G | A | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+6968C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626157 | |||||||
chr15:73626331 | G | C | 1 | a0001c0001t0001g0267 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.91+6794C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626331 | |||||||
chr15:73626431 | G | T | 1 | a0001c0001t0001g0244 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.91+6694C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626431 | |||||||
chr15:73626452 | C | T | 1 | a0001c0001t0002g0217 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.91+6673G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626452 | |||||||
chr15:73626458 | A | G | 1 | a0001c0001t0001g0276 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.91+6667T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626458 | |||||||
chr15:73626636 | T | C | 2 | a0001c0001t0001g0210 a0001c0001t0001g0211 |
2 | HG01346.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.91+6489A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73626636 | |||||||
chr15:73627107 | C | T | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.91+6018G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73627107 | |||||||
chr15:73627784 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.91+5341A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73627784 | |||||||
chr15:73628125 | G | A | 1 | a0001c0001t0004g0216 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.91+5000C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628125 | |||||||
chr15:73628227 | C | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0074 |
2 | NA18974.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.91+4898G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628227 | |||||||
chr15:73628229 | A | G | 24 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(21): Show |
34 | HG00609.hp2 HG00733.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.91+4896T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628229 | |||||||
chr15:73628260 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.91+4865C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628260 | |||||||
chr15:73628388 | T | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+4737A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628388 | |||||||
chr15:73628528 | C | G | 1 | a0001c0001t0001g0054 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.91+4597G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628528 | |||||||
chr15:73628607 | C | G | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+4518G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628607 | |||||||
chr15:73628866 | C | G | 9 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(6): Show |
9 | HG00438.hp1 HG02155.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.91+4259G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73628866 | |||||||
chr15:73629079 | C | T | 27 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(24): Show |
32 | HG00558.hp1 HG00639.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.91+4046G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629079 | |||||||
chr15:73629141 | G | C | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+3984C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629141 | |||||||
chr15:73629147 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.91+3978A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629147 | |||||||
chr15:73629216 | A | T | 1 | a0001c0001t0001g0053 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.91+3909T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629216 | |||||||
chr15:73629233 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+3892C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629233 | |||||||
chr15:73629479 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.91+3646G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629479 | |||||||
chr15:73629655 | T | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(68): Show |
85 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.91+3470A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629655 | |||||||
chr15:73629851 | A | G | 1 | a0001c0001t0001g0051 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.91+3274T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73629851 | |||||||
chr15:73630019 | G | A | 10 | a0001c0001t0002g0012 a0001c0001t0002g0030 a0001c0001t0002g0031 others(7): Show |
15 | HG01516.hp1 HG01517.hp2 HG02071.hp2 others(12): Show |
intron_variant | MODIFIER | c.91+3106C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630019 | |||||||
chr15:73630026 | T | C | 1 | a0001c0001t0001g0223 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.91+3099A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630026 | |||||||
chr15:73630185 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.91+2940T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630185 | |||||||
chr15:73630214 | G | C | 6 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0001g0226 others(3): Show |
6 | HG02055.hp2 HG02615.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+2911C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630214 | |||||||
chr15:73630266 | C | G | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.91+2859G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630266 | |||||||
chr15:73630402 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.91+2723G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630402 | |||||||
chr15:73630411 | A | T | 1 | a0001c0001t0001g0049 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.91+2714T>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630411 | |||||||
chr15:73630572 | T | C | 48 | a0001c0001t0001g0005 a0001c0001t0001g0034 a0001c0001t0001g0035 others(45): Show |
57 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.91+2553A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630572 | |||||||
chr15:73630630 | A | G | 4 | a0001c0001t0001g0045 a0001c0001t0001g0046 a0001c0001t0001g0047 others(1): Show |
4 | HG02559.hp1 NA18522.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.91+2495T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630630 | |||||||
chr15:73630667 | A | G | 6 | a0001c0001t0001g0238 a0001c0001t0001g0239 a0001c0001t0001g0240 others(3): Show |
6 | HG00438.hp1 HG04184.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.91+2458T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630667 | |||||||
chr15:73630830 | T | C | 1 | a0001c0001t0001g0232 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.91+2295A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630830 | |||||||
chr15:73630888 | G | C | 2 | a0001c0002t0001g0273 a0001c0002t0001g0274 |
2 | HG02280.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.91+2237C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630888 | |||||||
chr15:73630927 | T | A | 1 | a0001c0001t0001g0233 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.91+2198A>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73630927 | |||||||
chr15:73631248 | T | C | 1 | a0001c0001t0001g0033 | 2 | HG01081.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.91+1877A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631248 | |||||||
chr15:73631432 | C | G | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+1693G>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631432 | |||||||
chr15:73631509 | C | A | 2 | a0001c0001t0001g0234 a0001c0001t0001g0235 |
2 | HG02145.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.91+1616G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631509 | |||||||
chr15:73631711 | C | T | 2 | a0001c0001t0001g0044 a0001c0001t0006g0279 |
2 | HG01346.hp2 HG03491.hp2 |
intron_variant | MODIFIER | c.91+1414G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631711 | |||||||
chr15:73631881 | C | A | 2 | a0001c0001t0001g0236 a0001c0001t0001g0237 |
2 | HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.91+1244G>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631881 | |||||||
chr15:73631932 | A | G | 1 | a0001c0001t0001g0034 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.91+1193T>C | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73631932 | |||||||
chr15:73632110 | G | A | 45 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(42): Show |
51 | HG00438.hp1 HG00558.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.91+1015C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632110 | |||||||
chr15:73632538 | T | C | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+587A>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632538 | |||||||
chr15:73632931 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.91+194C>G | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632931 | |||||||
chr15:73632961 | C | T | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+164G>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73632961 | |||||||
chr15:73633052 | G | A | 4 | a0001c0001t0001g0039 a0001c0001t0001g0276 a0001c0001t0001g0277 others(1): Show |
5 | HG01243.hp2 HG01255.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.91+73C>T | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73633052 | |||||||
chr15:73633059 | G | T | 1 | a0001c0001t0001g0043 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.91+66C>A | NPTN | ENSG00000156642.17 | transcript | ENST00000345330.9 | protein_coding | 1/8 | chr15 | 73633059 |