Item | Value |
---|---|
geneid | 79096 |
ensemblid | ENSG00000149179.14 |
hgncid | 28720 |
symbol | CSTPP1 |
name | centriolar satellite-associated tubulin polyglutamylase complex regulator 1 |
refseq_nuc | NM_024113.5 |
refseq_prot | NP_077018.1 |
ensembl_nuc | ENST00000278460.12 |
ensembl_prot | ENSP00000278460.8 |
mane_status | MANE Select |
chr | chr11 |
start | 46936761 |
end | 47162247 |
strand | + |
ver | v1.2 |
region | chr11:46936761-47162247 |
region5000 | chr11:46931761-47167247 |
regionname0 | CSTPP1_chr11_46936761_47162247 |
regionname5000 | CSTPP1_chr11_46931761_47167247 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 331 | 218 | 70 | 53 | 64 | 4 | 25 | 49 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | MLSPE others(326): Show |
chr11 | 46931761 | 47167247 |
a0002 | 0/0 | 331 | 2 | 0 | 0 | 1 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | MLSPE others(326): Show |
chr11 | 46931761 | 47167247 |
a0003 | 0/0 | 331 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | MLSPE others(326): Show |
chr11 | 46931761 | 47167247 |
a0004 | 0/0 | 331 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | MLSPE others(326): Show |
chr11 | 46931761 | 47167247 |
a0005 | 0/0 | 117 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | MLSPE others(112): Show |
chr11 | 46931761 | 47167247 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 993 | 215 | 69 | 52 | 63 | 4 | 25 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0001c0004 | 0/0 | 993 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0001c0005 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0001c0007 | 0/0 | 993 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0002c0003 | 0/0 | 993 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0002c0009 | 0/0 | 993 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0003c0002 | 0/0 | 993 | 2 | 1 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0004c0006 | 0/0 | 993 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 | ||
a0005c0008 | 0/0 | 993 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | ATGCT others(988): Show |
chr11 | 46931761 | 47167247 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 1650 | 199 | 60 | 46 | 63 | 4 | 24 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0001c0001t0002 | 0/0 | 1650 | 10 | 8 | 2 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0001c0001t0003 | 0/0 | 1650 | 5 | 0 | 4 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0001c0001t0004 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0001c0004t0001 | 0/0 | 1650 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0001c0005t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0001c0007t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0002c0003t0001 | 0/0 | 1650 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0002c0009t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0003c0002t0001 | 0/0 | 1650 | 2 | 1 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0004c0006t0001 | 0/0 | 1650 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
a0005c0008t0001 | 0/0 | 1650 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | CCGGA others(1645): Show |
chr11 | 46931761 | 47167247 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0014 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0222 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0001t0004g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0004t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0005t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0001c0007t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0002c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0002c0009t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0003c0002t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0003c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0004c0006t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
a0005c0008t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | FIN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00609 | hp1 | a0002 | c0009 | t0001 | g0088 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0113 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01109 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0100 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01243 | hp2 | a0003 | c0002 | t0001 | g0086 | AMR | PUR | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0211 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0093 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | CLM | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0112 | EUR | IBS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0097 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | KHV | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0217 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CDX | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | CDX | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | PEL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02615 | hp1 | a0001 | c0001 | t0004 | g0220 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0210 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0129 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02895 | hp2 | a0004 | c0006 | t0001 | g0200 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0223 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0083 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0179 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0185 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0224 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | GWD | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0151 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0046 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG04184 | hp1 | a0002 | c0003 | t0001 | g0115 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | BEB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0181 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18951 | hp1 | a0005 | c0008 | t0001 | g0003 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18991 | hp2 | a0001 | c0007 | t0001 | g0063 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | LWK | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | LWK | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0209 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | YRI | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0215 | AFR | ASW | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ASW | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | MSL | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA20300 | hp1 | a0003 | c0002 | t0001 | g0087 | AFR | USA | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | USA | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0014 | REF | REF | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0222 | REF | REF | CSTPP1_chr11_46931761_47167247 | CSTPP1 | chr11 | 46931761 | 47167247 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47052476 | C | T | 1 | a0002 | 1 | HG00609.hp1 | missense_variant | MODERATE | c.238C>T | p.Arg80Trp | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/9 | 283/1650 | 238/996 | 80/331 | chr11 | 47052476 | |||
chr11:47052477 | G | A | 1 | a0002 | 1 | HG04184.hp1 | missense_variant | MODERATE | c.239G>A | p.Arg80Gln | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/9 | 284/1650 | 239/996 | 80/331 | chr11 | 47052477 | |||
chr11:47137716 | C | T | 1 | a0005 | 1 | NA18951.hp1 | stop_gained | HIGH | c.352C>T | p.Gln118* | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/9 | 397/1650 | 352/996 | 118/331 | chr11 | 47137716 | |||
chr11:47161161 | C | A | 1 | a0003 | 2 | HG01243.hp2 NA20300.hp1 |
missense_variant | MODERATE | c.792C>A | p.Asp264Glu | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/9 | 837/1650 | 792/996 | 264/331 | chr11 | 47161161 | |||
chr11:47161501 | G | A | 1 | a0004 | 1 | HG02895.hp2 | missense_variant | MODERATE | c.859G>A | p.Ala287Thr | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 904/1650 | 859/996 | 287/331 | chr11 | 47161501 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47137703 | G | A | 1 | a0001c0004 | 1 | HG01071.hp1 | synonymous_variant | LOW | c.339G>A | p.Pro113Pro | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/9 | 384/1650 | 339/996 | 113/331 | chr11 | 47137703 | |||
chr11:47157129 | T | C | 1 | a0001c0005 | 1 | HG02965.hp1 | synonymous_variant | LOW | c.558T>C | p.Pro186Pro | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/9 | 603/1650 | 558/996 | 186/331 | chr11 | 47157129 | |||
chr11:47161623 | C | T | 1 | a0001c0007 | 1 | NA18991.hp2 | synonymous_variant | LOW | c.981C>T | p.Asp327Asp | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 1026/1650 | 981/996 | 327/331 | chr11 | 47161623 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:47161825 | G | A | 1 | a0001c0001t0003 | 5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*187G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 187 | chr11 | 47161825 | ||||||
chr11:47162022 | G | A | 1 | a0001c0001t0002 | 10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*384G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 384 | chr11 | 47162022 | ||||||
chr11:47162032 | G | A | 1 | a0001c0001t0004 | 1 | HG02615.hp1 | 3_prime_UTR_variant | MODIFIER | c.*394G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 9/9 | 394 | chr11 | 47162032 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr11:46937116 | T | C | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.46+265T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937116 | |||||||
chr11:46937147 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.46+296T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937147 | |||||||
chr11:46937351 | GT | G | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.46+502delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46937351 | ||||||
chr11:46937738 | C | T | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+887C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937738 | |||||||
chr11:46937805 | T | G | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.46+954T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937805 | |||||||
chr11:46937820 | A | T | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46+969A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46937820 | |||||||
chr11:46937883 | C | CGTTTT | 6 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(3): Show |
6 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.46+1053_46+1057dup others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46937883 | ||||||
chr11:46938015 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.46+1164C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938015 | |||||||
chr11:46938493 | C | T | 1 | a0001c0001t0001g0075 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.46+1642C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938493 | |||||||
chr11:46938508 | TC | T | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.46+1661delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46938508 | ||||||
chr11:46938761 | C | CT | 19 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(16): Show |
19 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.46+1922dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46938761 | ||||||
chr11:46938771 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+1920T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938771 | |||||||
chr11:46938771 | T | TC | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+1920_46+1921ins others(1): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938771 | |||||||
chr11:46938780 | C | CT | 87 | a0001c0001t0001g0089 a0001c0001t0001g0090 a0001c0001t0001g0091 others(84): Show |
87 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(84): Show |
intron_variant | MODIFIER | c.46+1944dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46938780 | ||||||
chr11:46938837 | G | A | 2 | a0003c0002t0001g0086 a0003c0002t0001g0087 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.46+1986G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46938837 | |||||||
chr11:46939011 | A | C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.46+2160A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939011 | |||||||
chr11:46939082 | C | CT | 12 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0070 others(9): Show |
12 | HG00741.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.46+2256dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939082 | ||||||
chr11:46939082 | CT | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0074 others(7): Show |
10 | HG00609.hp1 HG01074.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+2256delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939082 | ||||||
chr11:46939259 | T | C | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+2408T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939259 | |||||||
chr11:46939282 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.46+2431T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939282 | |||||||
chr11:46939583 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.46+2732A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939583 | |||||||
chr11:46939631 | C | CATAG | 34 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(31): Show |
34 | HG00609.hp1 HG00609.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.46+2821_46+2824dup others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | ||||||
chr11:46939631 | C | CATAGATA others(1): Show |
3 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0090 |
3 | HG00621.hp1 HG02165.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.46+2817_46+2824dup others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | ||||||
chr11:46939631 | CATAG | C | 35 | a0001c0001t0001g0001 a0001c0001t0001g0054 a0001c0001t0001g0055 others(32): Show |
35 | HG01071.hp2 HG01074.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.46+2821_46+2824del others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | ||||||
chr11:46939631 | CATAGATA others(1): Show |
C | 4 | a0001c0001t0001g0067 a0001c0001t0001g0215 a0001c0001t0001g0216 others(1): Show |
4 | HG00735.hp2 HG03516.hp2 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.46+2817_46+2824del others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | ||||||
chr11:46939631 | CATAGATA others(5): Show |
C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.46+2813_46+2824del others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939631 | ||||||
chr11:46939668 | ATAGATAG others(1): Show |
A | 3 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0003c0002t0001g0087 |
3 | HG01358.hp2 HG03579.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.46+2823_46+2830del others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939668 | ||||||
chr11:46939672 | ATAGG | A | 53 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(50): Show |
53 | HG00438.hp1 HG00597.hp2 HG00673.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+2825_46+2828del others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939672 | ||||||
chr11:46939676 | G | A | 41 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(38): Show |
41 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(38): Show |
intron_variant | MODIFIER | c.46+2825G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46939676 | |||||||
chr11:46939831 | A | AT | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+2983dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46939831 | ||||||
chr11:46940208 | G | A | 1 | a0001c0001t0001g0089 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.46+3357G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940208 | |||||||
chr11:46940444 | T | C | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(2): Show |
5 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+3593T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940444 | |||||||
chr11:46940635 | C | CTA | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+3793_46+3794dup others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46940635 | ||||||
chr11:46940684 | G | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46+3833G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940684 | |||||||
chr11:46940736 | T | G | 1 | a0001c0001t0001g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.46+3885T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940736 | |||||||
chr11:46940900 | T | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
66 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(63): Show |
intron_variant | MODIFIER | c.46+4049T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940900 | |||||||
chr11:46940923 | G | T | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+4072G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46940923 | |||||||
chr11:46941485 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.46+4634A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46941485 | |||||||
chr11:46941645 | A | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
164 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.46+4794A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46941645 | |||||||
chr11:46942496 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.46+5645G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942496 | |||||||
chr11:46942520 | A | G | 1 | a0001c0001t0002g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.46+5669A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942520 | |||||||
chr11:46942609 | C | T | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+5758C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942609 | |||||||
chr11:46942800 | T | C | 4 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(1): Show |
4 | HG02809.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+5949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46942800 | |||||||
chr11:46943283 | C | G | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+6432C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943283 | |||||||
chr11:46943760 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.46+6909C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943760 | |||||||
chr11:46943920 | C | T | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+7069C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943920 | |||||||
chr11:46943975 | C | T | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+7124C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46943975 | |||||||
chr11:46944179 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.46+7328G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944179 | |||||||
chr11:46944317 | C | CA | 49 | a0001c0001t0001g0012 a0001c0001t0001g0054 a0001c0001t0001g0067 others(46): Show |
49 | HG00735.hp2 HG00741.hp1 HG01109.hp1 others(46): Show |
intron_variant | MODIFIER | c.46+7485dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46944317 | ||||||
chr11:46944405 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.46+7554A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944405 | |||||||
chr11:46944662 | C | A | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.46+7811C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944662 | |||||||
chr11:46944800 | T | C | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.46+7949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944800 | |||||||
chr11:46944942 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.46+8091A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46944942 | |||||||
chr11:46945082 | T | C | 3 | a0001c0001t0001g0055 a0001c0001t0001g0067 a0001c0001t0001g0074 |
3 | HG00735.hp2 HG01257.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.46+8231T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945082 | |||||||
chr11:46945218 | A | C | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.46+8367A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945218 | |||||||
chr11:46945257 | G | A | 14 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0109 others(11): Show |
14 | HG00609.hp1 HG01071.hp1 HG01099.hp2 others(11): Show |
intron_variant | MODIFIER | c.46+8406G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945257 | |||||||
chr11:46945353 | G | A | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.46+8502G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945353 | |||||||
chr11:46945354 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+8503C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945354 | |||||||
chr11:46945412 | C | T | 2 | a0001c0001t0001g0106 a0001c0001t0001g0165 |
2 | HG00738.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.46+8561C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945412 | |||||||
chr11:46945530 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.46+8679G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945530 | |||||||
chr11:46945593 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.46+8742C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945593 | |||||||
chr11:46945864 | T | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
56 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.46+9013T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46945864 | |||||||
chr11:46946058 | T | C | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+9207T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946058 | |||||||
chr11:46946111 | C | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.46+9260C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946111 | |||||||
chr11:46946128 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.46+9277C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946128 | |||||||
chr11:46946159 | G | T | 1 | a0001c0001t0001g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.46+9308G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946159 | |||||||
chr11:46946336 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.46+9485C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946336 | |||||||
chr11:46946350 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.46+9499G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946350 | |||||||
chr11:46946455 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+9604G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46946455 | |||||||
chr11:46947272 | C | G | 3 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0002c0009t0001g0088 |
3 | HG00609.hp1 NA18971.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.46+10421C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947272 | |||||||
chr11:46947730 | C | G | 56 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(53): Show |
56 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.46+10879C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947730 | |||||||
chr11:46947737 | C | T | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.46+10886C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46947737 | |||||||
chr11:46947928 | C | CT | 17 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(14): Show |
17 | HG00438.hp2 HG00597.hp2 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.46+11088dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46947928 | ||||||
chr11:46948065 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.46+11214T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948065 | |||||||
chr11:46948217 | G | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0162 |
3 | HG03942.hp1 NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.46+11366G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948217 | |||||||
chr11:46948348 | G | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0064 |
2 | HG01261.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.46+11497G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948348 | |||||||
chr11:46948880 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.46+12029A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948880 | |||||||
chr11:46948931 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.46+12080G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46948931 | |||||||
chr11:46949025 | A | T | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.46+12174A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949025 | |||||||
chr11:46949343 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.46+12492C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949343 | |||||||
chr11:46949415 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.46+12564C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949415 | |||||||
chr11:46949669 | C | CT | 49 | a0001c0001t0001g0035 a0001c0001t0001g0053 a0001c0001t0001g0075 others(46): Show |
49 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.46+12834dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46949669 | ||||||
chr11:46949669 | CT | C | 26 | a0001c0001t0001g0120 a0001c0001t0001g0191 a0001c0001t0001g0192 others(23): Show |
26 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.46+12834delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46949669 | ||||||
chr11:46949888 | G | T | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46+13037G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949888 | |||||||
chr11:46949889 | T | G | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.46+13038T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949889 | |||||||
chr11:46949920 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46+13069G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949920 | |||||||
chr11:46949988 | T | C | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+13137T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46949988 | |||||||
chr11:46950176 | C | CT | 49 | a0001c0001t0001g0076 a0001c0001t0001g0155 a0001c0001t0001g0156 others(46): Show |
49 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(46): Show |
intron_variant | MODIFIER | c.46+13340dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46950176 | ||||||
chr11:46950229 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+13378A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950229 | |||||||
chr11:46950235 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.46+13384G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950235 | |||||||
chr11:46950318 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.46+13467C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950318 | |||||||
chr11:46950363 | C | T | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0219 |
3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.46+13512C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950363 | |||||||
chr11:46950394 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+13543C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950394 | |||||||
chr11:46950614 | C | T | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.46+13763C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950614 | |||||||
chr11:46950824 | C | A | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+13973C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950824 | |||||||
chr11:46950867 | G | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.46+14016G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950867 | |||||||
chr11:46950905 | C | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.46+14054C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46950905 | |||||||
chr11:46951295 | CT | C | 46 | a0001c0001t0001g0048 a0001c0001t0001g0056 a0001c0001t0001g0076 others(43): Show |
46 | HG01109.hp1 HG01109.hp2 HG01261.hp1 others(43): Show |
intron_variant | MODIFIER | c.46+14463delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46951295 | ||||||
chr11:46951474 | CTTTG | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0054 others(2): Show |
5 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+14630_46+14633d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46951474 | ||||||
chr11:46951564 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.46+14713C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46951564 | |||||||
chr11:46951906 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.46+15055C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46951906 | |||||||
chr11:46952250 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.46+15399G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46952250 | |||||||
chr11:46952794 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+15943C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46952794 | |||||||
chr11:46953093 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.46+16242A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953093 | |||||||
chr11:46953558 | A | C | 1 | a0001c0001t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.46+16707A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953558 | |||||||
chr11:46953574 | T | C | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+16723T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953574 | |||||||
chr11:46953836 | G | A | 164 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(161): Show |
164 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(161): Show |
intron_variant | MODIFIER | c.46+16985G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46953836 | |||||||
chr11:46954206 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.46+17355T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954206 | |||||||
chr11:46954434 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.46+17583G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954434 | |||||||
chr11:46954497 | C | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+17646C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954497 | |||||||
chr11:46954556 | T | A | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.46+17705T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954556 | |||||||
chr11:46954565 | A | G | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+17714A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954565 | |||||||
chr11:46954798 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.46+17947C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954798 | |||||||
chr11:46954802 | C | A | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.46+17951C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46954802 | |||||||
chr11:46955310 | G | T | 58 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(55): Show |
58 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.46+18459G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955310 | |||||||
chr11:46955347 | G | GT | 5 | a0001c0001t0001g0061 a0001c0001t0001g0081 a0001c0001t0001g0108 others(2): Show |
5 | HG00735.hp1 HG01981.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+18506dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955347 | ||||||
chr11:46955369 | G | T | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+18518G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955369 | |||||||
chr11:46955390 | G | A | 156 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(153): Show |
156 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.46+18539G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955390 | |||||||
chr11:46955450 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.46+18599G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955450 | |||||||
chr11:46955475 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+18624C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955475 | |||||||
chr11:46955516 | A | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.46+18665A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955516 | |||||||
chr11:46955609 | C | T | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.46+18758C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955609 | |||||||
chr11:46955739 | C | G | 1 | a0001c0001t0001g0103 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.46+18888C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955739 | |||||||
chr11:46955857 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+19006C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955857 | |||||||
chr11:46955858 | G | A | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.46+19007G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955858 | |||||||
chr11:46955986 | A | AC | 15 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0008 others(12): Show |
15 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.46+19148dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955986 | ||||||
chr11:46955986 | AC | A | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(117): Show |
120 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.46+19148delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955986 | ||||||
chr11:46955986 | ACC | A | 33 | a0001c0001t0001g0056 a0001c0001t0001g0073 a0001c0001t0001g0077 others(30): Show |
33 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.46+19147_46+19148d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46955986 | ||||||
chr11:46955990 | C | A | 4 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0184 others(1): Show |
4 | HG00609.hp1 HG01243.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+19139C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955990 | |||||||
chr11:46955991 | C | A | 2 | a0001c0001t0001g0036 a0001c0001t0002g0217 |
2 | HG02145.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.46+19140C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955991 | |||||||
chr11:46955994 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.46+19143C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955994 | |||||||
chr11:46955994 | C | G | 3 | a0001c0001t0001g0084 a0001c0001t0001g0127 a0001c0001t0001g0169 |
3 | HG03017.hp2 NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.46+19143C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955994 | |||||||
chr11:46955995 | C | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+19144C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46955995 | |||||||
chr11:46956118 | A | C | 1 | a0001c0001t0001g0104 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.46+19267A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956118 | |||||||
chr11:46956144 | T | G | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.46+19293T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956144 | |||||||
chr11:46956331 | A | C | 58 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(55): Show |
58 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.46+19480A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956331 | |||||||
chr11:46956371 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0054 others(2): Show |
5 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+19520A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956371 | |||||||
chr11:46956553 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+19702A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46956553 | |||||||
chr11:46956676 | A | AT | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.46+19834dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46956676 | ||||||
chr11:46957024 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.46+20173G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957024 | |||||||
chr11:46957147 | G | A | 148 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+20296G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957147 | |||||||
chr11:46957344 | C | G | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+20493C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957344 | |||||||
chr11:46957472 | A | G | 148 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+20621A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957472 | |||||||
chr11:46957547 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.46+20696T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957547 | |||||||
chr11:46957587 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.46+20736A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957587 | |||||||
chr11:46957837 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.46+20986C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957837 | |||||||
chr11:46957879 | C | T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0101 |
2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.46+21028C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957879 | |||||||
chr11:46957914 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.46+21063G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957914 | |||||||
chr11:46957937 | T | C | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.46+21086T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46957937 | |||||||
chr11:46958143 | G | C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.46+21292G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958143 | |||||||
chr11:46958397 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+21546G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958397 | |||||||
chr11:46958535 | C | T | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.46+21684C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958535 | |||||||
chr11:46958753 | CT | C | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.46+21904delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46958753 | ||||||
chr11:46958885 | C | T | 1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.46+22034C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958885 | |||||||
chr11:46958952 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.46+22101A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46958952 | |||||||
chr11:46959202 | G | GT | 6 | a0001c0001t0001g0035 a0001c0001t0001g0072 a0001c0001t0001g0081 others(3): Show |
6 | HG02293.hp1 HG02293.hp2 HG02300.hp1 others(3): Show |
intron_variant | MODIFIER | c.46+22362dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46959202 | ||||||
chr11:46959588 | C | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0126 |
3 | NA18949.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.46+22737C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46959588 | |||||||
chr11:46959641 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.46+22790T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46959641 | |||||||
chr11:46959865 | A | AT | 50 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0126 others(47): Show |
50 | HG01109.hp2 HG01243.hp1 HG01261.hp1 others(47): Show |
intron_variant | MODIFIER | c.46+23033dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46959865 | ||||||
chr11:46959865 | AT | A | 5 | a0001c0001t0001g0017 a0001c0001t0001g0036 a0001c0001t0001g0090 others(2): Show |
5 | HG00738.hp1 NA18960.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+23033delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46959865 | ||||||
chr11:46960095 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(163): Show |
166 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.46+23244A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960095 | |||||||
chr11:46960587 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.46+23736G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960587 | |||||||
chr11:46960612 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+23761A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960612 | |||||||
chr11:46960724 | T | C | 148 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+23873T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960724 | |||||||
chr11:46960861 | G | A | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+24010G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960861 | |||||||
chr11:46960861 | GA | G | 43 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(40): Show |
43 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(40): Show |
intron_variant | MODIFIER | c.46+24021delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46960861 | ||||||
chr11:46960862 | A | G | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.46+24011A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960862 | |||||||
chr11:46960911 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.46+24060C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960911 | |||||||
chr11:46960930 | G | A | 148 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.46+24079G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960930 | |||||||
chr11:46960965 | C | T | 4 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0059 others(1): Show |
4 | HG00280.hp1 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+24114C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46960965 | |||||||
chr11:46961009 | T | C | 2 | a0001c0001t0001g0084 a0001c0001t0001g0127 |
2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.46+24158T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46961009 | |||||||
chr11:46961227 | CTTG | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.46+24386_46+24388d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46961227 | ||||||
chr11:46961687 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.46+24836A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46961687 | |||||||
chr11:46961708 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.46+24857T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46961708 | |||||||
chr11:46962089 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-25119A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962089 | |||||||
chr11:46962130 | C | T | 2 | a0001c0001t0001g0084 a0001c0001t0001g0127 |
2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.47-25078C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962130 | |||||||
chr11:46962303 | CT | C | 2 | a0001c0001t0002g0205 a0001c0001t0002g0218 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.47-24903delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46962303 | ||||||
chr11:46962571 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.47-24637G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962571 | |||||||
chr11:46962616 | C | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-24592C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962616 | |||||||
chr11:46962770 | T | C | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.47-24438T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962770 | |||||||
chr11:46962935 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-24273C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46962935 | |||||||
chr11:46963078 | C | T | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-24130C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963078 | |||||||
chr11:46963106 | AT | A | 17 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0102 others(14): Show |
17 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-24092delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963106 | ||||||
chr11:46963252 | A | G | 155 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(152): Show |
155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.47-23956A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963252 | |||||||
chr11:46963324 | CT | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-23869delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963324 | ||||||
chr11:46963558 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-23650C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963558 | |||||||
chr11:46963628 | C | CA | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-23572dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963628 | ||||||
chr11:46963679 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.47-23529G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963679 | |||||||
chr11:46963724 | G | C | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.47-23484G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46963724 | |||||||
chr11:46963784 | C | CA | 35 | a0001c0001t0001g0011 a0001c0001t0001g0066 a0001c0001t0001g0172 others(32): Show |
35 | HG01109.hp1 HG01243.hp1 HG01261.hp1 others(32): Show |
intron_variant | MODIFIER | c.47-23408dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46963784 | ||||||
chr11:46964148 | C | G | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.47-23060C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964148 | |||||||
chr11:46964289 | CT | C | 50 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(47): Show |
50 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(47): Show |
intron_variant | MODIFIER | c.47-22905delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46964289 | ||||||
chr11:46964291 | T | C | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.47-22917T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964291 | |||||||
chr11:46964386 | C | G | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.47-22822C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964386 | |||||||
chr11:46964510 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-22698C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964510 | |||||||
chr11:46964576 | C | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-22632C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964576 | |||||||
chr11:46964887 | G | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-22321G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46964887 | |||||||
chr11:46965220 | C | CT | 13 | a0001c0001t0001g0084 a0001c0001t0001g0092 a0001c0001t0001g0104 others(10): Show |
13 | HG00673.hp1 HG01192.hp1 HG01981.hp2 others(10): Show |
intron_variant | MODIFIER | c.47-21976dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46965220 | ||||||
chr11:46965231 | TTA | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-21975_47-21974d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46965231 | ||||||
chr11:46965232 | TA | T | 41 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(38): Show |
41 | HG00280.hp2 HG01109.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.47-21975delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965232 | |||||||
chr11:46965233 | A | T | 89 | a0001c0001t0001g0077 a0001c0001t0001g0082 a0001c0001t0001g0084 others(86): Show |
89 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.47-21975A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965233 | |||||||
chr11:46965367 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-21841G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965367 | |||||||
chr11:46965424 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0094 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-21784C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965424 | |||||||
chr11:46965444 | T | C | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-21764T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965444 | |||||||
chr11:46965848 | G | A | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.47-21360G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965848 | |||||||
chr11:46965936 | A | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-21272A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46965936 | |||||||
chr11:46966135 | C | T | 1 | a0001c0001t0001g0044 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.47-21073C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966135 | |||||||
chr11:46966150 | C | G | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-21058C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966150 | |||||||
chr11:46966153 | C | T | 48 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(45): Show |
48 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.47-21055C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966153 | |||||||
chr11:46966292 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.47-20916C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966292 | |||||||
chr11:46966299 | C | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-20909C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966299 | |||||||
chr11:46966402 | T | A | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.47-20806T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966402 | |||||||
chr11:46966429 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-20779G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966429 | |||||||
chr11:46966645 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.47-20563G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46966645 | |||||||
chr11:46967000 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.47-20208A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967000 | |||||||
chr11:46967282 | T | C | 2 | a0001c0001t0001g0192 a0004c0006t0001g0200 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.47-19926T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967282 | |||||||
chr11:46967432 | A | C | 91 | a0001c0001t0001g0031 a0001c0001t0001g0082 a0001c0001t0001g0084 others(88): Show |
91 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(88): Show |
intron_variant | MODIFIER | c.47-19776A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967432 | |||||||
chr11:46967466 | A | G | 1 | a0001c0001t0001g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.47-19742A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967466 | |||||||
chr11:46967831 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.47-19377C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967831 | |||||||
chr11:46967945 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.47-19263C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46967945 | |||||||
chr11:46968282 | G | C | 2 | a0001c0001t0001g0192 a0004c0006t0001g0200 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.47-18926G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968282 | |||||||
chr11:46968789 | C | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-18419C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968789 | |||||||
chr11:46968813 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.47-18395C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968813 | |||||||
chr11:46968815 | C | G | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-18393C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968815 | |||||||
chr11:46968911 | A | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0094 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-18297A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968911 | |||||||
chr11:46968913 | A | T | 3 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0126 |
3 | NA18949.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.47-18295A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46968913 | |||||||
chr11:46969036 | C | T | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-18172C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969036 | |||||||
chr11:46969074 | A | C | 2 | a0001c0001t0001g0130 a0001c0001t0001g0151 |
2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.47-18134A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969074 | |||||||
chr11:46969103 | T | A | 1 | a0001c0001t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.47-18105T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969103 | |||||||
chr11:46969144 | C | A | 8 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0120 others(5): Show |
8 | HG00621.hp2 HG02080.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-18064C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969144 | |||||||
chr11:46969152 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-18056C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969152 | |||||||
chr11:46969656 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.47-17552G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969656 | |||||||
chr11:46969693 | T | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-17515T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46969693 | |||||||
chr11:46970011 | A | G | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-17197A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970011 | |||||||
chr11:46970064 | T | C | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.47-17144T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970064 | |||||||
chr11:46970257 | C | T | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0170 others(1): Show |
4 | HG01071.hp1 HG01515.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-16951C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970257 | |||||||
chr11:46970271 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.47-16937C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46970271 | |||||||
chr11:46970402 | T | TAATA | 6 | a0001c0001t0001g0140 a0001c0001t0001g0221 a0001c0001t0001g0223 others(3): Show |
6 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.47-16779_47-16776d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46970402 | ||||||
chr11:46971221 | C | T | 1 | a0001c0001t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.47-15987C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971221 | |||||||
chr11:46971243 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.47-15965T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971243 | |||||||
chr11:46971257 | G | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-15951G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971257 | |||||||
chr11:46971279 | T | A | 1 | a0001c0001t0001g0037 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.47-15929T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971279 | |||||||
chr11:46971493 | T | C | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.47-15715T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971493 | |||||||
chr11:46971644 | AT | A | 11 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(8): Show |
11 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(8): Show |
intron_variant | MODIFIER | c.47-15552delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46971644 | ||||||
chr11:46971921 | A | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-15287A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46971921 | |||||||
chr11:46972634 | C | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-14574C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46972634 | |||||||
chr11:46972728 | C | A | 2 | a0001c0001t0001g0054 a0001c0001t0001g0064 |
2 | HG01261.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.47-14480C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46972728 | |||||||
chr11:46973163 | A | G | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-14045A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973163 | |||||||
chr11:46973242 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-13966G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973242 | |||||||
chr11:46973448 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47-13760C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973448 | |||||||
chr11:46973755 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.47-13453C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46973755 | |||||||
chr11:46973780 | A | ATGTGTG | 72 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(69): Show |
72 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.47-13414_47-13409d others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | ||||||
chr11:46973780 | A | ATGTGTGT others(3): Show |
78 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(75): Show |
78 | HG00735.hp2 HG01074.hp1 HG01109.hp2 others(75): Show |
intron_variant | MODIFIER | c.47-13418_47-13409d others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | ||||||
chr11:46973780 | A | ATGTGTGT others(5): Show |
10 | a0001c0001t0001g0081 a0001c0001t0001g0094 a0001c0001t0001g0121 others(7): Show |
10 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-13420_47-13409d others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | ||||||
chr11:46973780 | A | ATGTGTGT others(7): Show |
1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.47-13422_47-13409d others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | ||||||
chr11:46973780 | A | ATGTGTGT others(11): Show |
2 | a0001c0001t0001g0221 a0001c0005t0001g0083 |
2 | HG02965.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.47-13426_47-13409d others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | ||||||
chr11:46973780 | A | ATGTGTGT others(13): Show |
2 | a0001c0001t0001g0223 a0001c0001t0001g0224 |
2 | HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.47-13409_47-13408i others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46973780 | ||||||
chr11:46974266 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.47-12942G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974266 | |||||||
chr11:46974298 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-12910C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974298 | |||||||
chr11:46974514 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.47-12694G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974514 | |||||||
chr11:46974526 | C | CA | 78 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(75): Show |
78 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(75): Show |
intron_variant | MODIFIER | c.47-12666dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974526 | ||||||
chr11:46974526 | C | CAA | 19 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0094 others(16): Show |
19 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.47-12667_47-12666d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974526 | ||||||
chr11:46974526 | CA | C | 30 | a0001c0001t0001g0178 a0001c0001t0001g0191 a0001c0001t0001g0192 others(27): Show |
30 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(27): Show |
intron_variant | MODIFIER | c.47-12666delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974526 | ||||||
chr11:46974568 | T | C | 58 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(55): Show |
58 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(55): Show |
intron_variant | MODIFIER | c.47-12640T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974568 | |||||||
chr11:46974593 | C | T | 17 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0094 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.47-12615C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974593 | |||||||
chr11:46974837 | A | C | 1 | a0001c0001t0001g0198 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.47-12371A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974837 | |||||||
chr11:46974857 | A | AAC | 22 | a0001c0001t0001g0011 a0001c0001t0001g0013 a0001c0001t0001g0017 others(19): Show |
22 | HG00280.hp1 HG00438.hp2 HG00741.hp1 others(19): Show |
intron_variant | MODIFIER | c.47-12305_47-12304d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | A | AACAC | 8 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0058 others(5): Show |
8 | HG01192.hp2 HG03831.hp1 NA18949.hp2 others(5): Show |
intron_variant | MODIFIER | c.47-12307_47-12304d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | AAC | A | 6 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0055 others(3): Show |
6 | HG00735.hp2 HG01257.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.47-12305_47-12304d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | AACAC | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0048 others(7): Show |
10 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.47-12307_47-12304d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | AACACACA others(1): Show |
A | 5 | a0001c0001t0001g0051 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02723.hp2 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-12311_47-12304d others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | AACACACA others(3): Show |
A | 16 | a0001c0001t0001g0077 a0001c0001t0001g0081 a0001c0001t0001g0094 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.47-12313_47-12304d others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | AACACACA others(5): Show |
A | 38 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0107 others(35): Show |
38 | HG01109.hp2 HG01243.hp2 HG01358.hp1 others(35): Show |
intron_variant | MODIFIER | c.47-12315_47-12304d others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974857 | AACACACA others(7): Show |
A | 89 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(86): Show |
89 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(86): Show |
intron_variant | MODIFIER | c.47-12317_47-12304d others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46974857 | ||||||
chr11:46974892 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-12316A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974892 | |||||||
chr11:46974893 | C | T | 2 | a0001c0001t0001g0112 a0001c0004t0001g0113 |
2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.47-12315C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46974893 | |||||||
chr11:46975047 | G | GC | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-12160dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46975047 | ||||||
chr11:46975049 | T | C | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-12159T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975049 | |||||||
chr11:46975657 | G | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.47-11551G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975657 | |||||||
chr11:46975676 | T | C | 1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.47-11532T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975676 | |||||||
chr11:46975919 | G | A | 1 | a0001c0001t0001g0033 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.47-11289G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46975919 | |||||||
chr11:46976100 | G | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-11108G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976100 | |||||||
chr11:46976393 | T | TCA | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
68 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.47-10786_47-10785d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | ||||||
chr11:46976393 | T | TCACA | 8 | a0001c0001t0001g0010 a0001c0001t0001g0017 a0001c0001t0001g0023 others(5): Show |
8 | HG00741.hp1 HG02280.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.47-10788_47-10785d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | ||||||
chr11:46976393 | TCA | T | 28 | a0001c0001t0001g0045 a0001c0001t0001g0077 a0001c0001t0001g0085 others(25): Show |
28 | HG00438.hp1 HG01109.hp1 HG01109.hp2 others(25): Show |
intron_variant | MODIFIER | c.47-10786_47-10785d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | ||||||
chr11:46976393 | TCACA | T | 100 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(97): Show |
100 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(97): Show |
intron_variant | MODIFIER | c.47-10788_47-10785d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | ||||||
chr11:46976393 | TCACACA | T | 12 | a0001c0001t0001g0076 a0001c0001t0001g0139 a0001c0001t0001g0174 others(9): Show |
12 | HG01975.hp2 HG02451.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.47-10790_47-10785d others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | ||||||
chr11:46976393 | TCACACAC others(1): Show |
T | 2 | a0001c0001t0001g0095 a0001c0001t0001g0101 |
2 | NA18973.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.47-10792_47-10785d others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976393 | ||||||
chr11:46976626 | A | C | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.47-10582A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976626 | |||||||
chr11:46976718 | TATGCAGT others(5): Show |
T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.47-10486_47-10475d others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46976718 | ||||||
chr11:46976936 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.47-10272G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976936 | |||||||
chr11:46976961 | T | C | 155 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(152): Show |
155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.47-10247T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46976961 | |||||||
chr11:46977305 | C | T | 1 | a0001c0007t0001g0063 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.47-9903C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977305 | |||||||
chr11:46977364 | T | C | 7 | a0001c0001t0001g0095 a0001c0001t0001g0101 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-9844T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977364 | |||||||
chr11:46977396 | T | A | 25 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0095 others(22): Show |
25 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-9812T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977396 | |||||||
chr11:46977469 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-9739T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46977469 | |||||||
chr11:46978287 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.47-8921G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978287 | |||||||
chr11:46978464 | T | A | 1 | a0001c0001t0001g0019 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.47-8744T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978464 | |||||||
chr11:46978470 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47-8738G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978470 | |||||||
chr11:46978671 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-8537T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46978671 | |||||||
chr11:46979023 | A | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-8185A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979023 | |||||||
chr11:46979387 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.47-7821C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979387 | |||||||
chr11:46979660 | C | T | 46 | a0001c0001t0001g0002 a0001c0001t0001g0082 a0001c0001t0001g0085 others(43): Show |
46 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.47-7548C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979660 | |||||||
chr11:46979863 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.47-7345C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46979863 | |||||||
chr11:46980081 | A | C | 54 | a0001c0001t0001g0010 a0001c0001t0001g0076 a0001c0001t0001g0077 others(51): Show |
54 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.47-7127A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980081 | |||||||
chr11:46980084 | A | C | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.47-7124A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980084 | |||||||
chr11:46980357 | C | G | 72 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(69): Show |
72 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(69): Show |
intron_variant | MODIFIER | c.47-6851C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980357 | |||||||
chr11:46980454 | C | A | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-6754C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980454 | |||||||
chr11:46980606 | C | G | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-6602C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46980606 | |||||||
chr11:46981021 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.47-6187G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981021 | |||||||
chr11:46981063 | A | T | 148 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.47-6145A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981063 | |||||||
chr11:46981335 | A | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-5873A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981335 | |||||||
chr11:46981638 | T | TTTTTGAG others(6): Show |
1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-5570_47-5569ins others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981638 | |||||||
chr11:46981639 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.47-5569G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981639 | |||||||
chr11:46981692 | T | G | 26 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(23): Show |
26 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.47-5516T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981692 | |||||||
chr11:46981730 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.47-5478G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981730 | |||||||
chr11:46981753 | G | A | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.47-5455G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981753 | |||||||
chr11:46981759 | A | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-5449A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981759 | |||||||
chr11:46981766 | T | A | 148 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.47-5442T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46981766 | |||||||
chr11:46982130 | A | T | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-5078A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982130 | |||||||
chr11:46982413 | CTTAG | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.47-4791_47-4788del others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46982413 | ||||||
chr11:46982436 | T | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-4772T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982436 | |||||||
chr11:46982458 | A | T | 1 | a0001c0001t0001g0144 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.47-4750A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982458 | |||||||
chr11:46982941 | G | A | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-4267G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46982941 | |||||||
chr11:46983034 | A | C | 9 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(6): Show |
9 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.47-4174A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983034 | |||||||
chr11:46983049 | A | G | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.47-4159A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983049 | |||||||
chr11:46983583 | G | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.47-3625G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983583 | |||||||
chr11:46983817 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.47-3391G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46983817 | |||||||
chr11:46984082 | G | A | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-3126G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46984082 | |||||||
chr11:46984517 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.47-2691G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46984517 | |||||||
chr11:46984586 | C | CT | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-2613dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46984586 | ||||||
chr11:46984880 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-2328T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46984880 | |||||||
chr11:46985051 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.47-2157T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985051 | |||||||
chr11:46985055 | G | A | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.47-2153G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985055 | |||||||
chr11:46985216 | G | C | 2 | a0001c0001t0001g0076 a0001c0001t0001g0183 |
2 | HG02451.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.47-1992G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985216 | |||||||
chr11:46985220 | G | A | 48 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(45): Show |
48 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(45): Show |
intron_variant | MODIFIER | c.47-1988G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985220 | |||||||
chr11:46985242 | C | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.47-1966C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985242 | |||||||
chr11:46985263 | G | C | 16 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.47-1945G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985263 | |||||||
chr11:46985580 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.47-1628C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46985580 | |||||||
chr11:46986045 | A | G | 1 | a0004c0006t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.47-1163A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986045 | |||||||
chr11:46986048 | A | T | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.47-1160A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986048 | |||||||
chr11:46986153 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.47-1055A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986153 | |||||||
chr11:46986370 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.47-838C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986370 | |||||||
chr11:46986399 | A | T | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.47-809A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986399 | |||||||
chr11:46986423 | CT | C | 38 | a0001c0001t0001g0046 a0001c0001t0001g0071 a0001c0001t0001g0076 others(35): Show |
38 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(35): Show |
intron_variant | MODIFIER | c.47-770delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr11 | 46986423 | ||||||
chr11:46986574 | C | T | 18 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0094 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.47-634C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986574 | |||||||
chr11:46986579 | C | A | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.47-629C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986579 | |||||||
chr11:46986828 | A | G | 97 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(94): Show |
97 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(94): Show |
intron_variant | MODIFIER | c.47-380A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 1/8 | chr11 | 46986828 | |||||||
chr11:46987490 | G | GT | 166 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(163): Show |
166 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.149+183dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46987490 | ||||||
chr11:46987773 | C | A | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+463C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46987773 | |||||||
chr11:46987838 | ATATAAGG others(3568): Show |
A | 1 | a0001c0001t0001g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.149+530_149+4104de others(1): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46987838 | ||||||
chr11:46987900 | A | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+590A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46987900 | |||||||
chr11:46988309 | C | T | 29 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(26): Show |
29 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.149+999C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988309 | |||||||
chr11:46988613 | C | CA | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(213): Show |
216 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.149+1309dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46988613 | ||||||
chr11:46988823 | A | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+1513A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988823 | |||||||
chr11:46988882 | T | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0221 a0001c0001t0001g0223 others(3): Show |
6 | HG02559.hp1 HG02615.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.149+1572T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988882 | |||||||
chr11:46988887 | T | A | 2 | a0001c0001t0001g0049 a0001c0001t0001g0050 |
2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.149+1577T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988887 | |||||||
chr11:46988940 | G | A | 17 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(14): Show |
17 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+1630G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46988940 | |||||||
chr11:46989145 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.149+1835G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989145 | |||||||
chr11:46989537 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+2227G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989537 | |||||||
chr11:46989567 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0001c0001t0001g0127 others(1): Show |
4 | NA18960.hp2 NA18964.hp1 NA18978.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+2257T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989567 | |||||||
chr11:46989878 | A | G | 154 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(151): Show |
154 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(151): Show |
intron_variant | MODIFIER | c.149+2568A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46989878 | |||||||
chr11:46990033 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+2723T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46990033 | |||||||
chr11:46991196 | GT | G | 132 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(129): Show |
132 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(129): Show |
intron_variant | MODIFIER | c.149+3903delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46991196 | ||||||
chr11:46991376 | G | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.149+4066G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991376 | |||||||
chr11:46991803 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.149+4493C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991803 | |||||||
chr11:46991834 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+4524G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991834 | |||||||
chr11:46991834 | G | T | 1 | a0001c0001t0001g0197 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.149+4524G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991834 | |||||||
chr11:46991890 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+4580G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991890 | |||||||
chr11:46991922 | C | G | 155 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(152): Show |
155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.149+4612C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991922 | |||||||
chr11:46991927 | GACGGGGT others(80): Show |
G | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.149+4619_149+4705d others(89): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46991927 | ||||||
chr11:46991929 | C | T | 46 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(43): Show |
46 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(43): Show |
intron_variant | MODIFIER | c.149+4619C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991929 | |||||||
chr11:46991930 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.149+4620G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46991930 | |||||||
chr11:46992017 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.149+4707A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992017 | |||||||
chr11:46992362 | A | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+5052A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992362 | |||||||
chr11:46992384 | C | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+5074C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992384 | |||||||
chr11:46992516 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.149+5206G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992516 | |||||||
chr11:46992541 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+5231A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992541 | |||||||
chr11:46992629 | G | A | 3 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0167 |
3 | HG00738.hp2 HG01358.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.149+5319G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992629 | |||||||
chr11:46992665 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0167 |
3 | HG00738.hp2 HG01358.hp2 HG02055.hp1 |
intron_variant | MODIFIER | c.149+5355C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46992665 | |||||||
chr11:46992972 | G | GT | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+5664dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46992972 | ||||||
chr11:46993500 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0008 |
2 | HG00609.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.149+6190G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993500 | |||||||
chr11:46993622 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+6312T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993622 | |||||||
chr11:46993745 | G | T | 90 | a0001c0001t0001g0082 a0001c0001t0001g0084 a0001c0001t0001g0085 others(87): Show |
90 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(87): Show |
intron_variant | MODIFIER | c.149+6435G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993745 | |||||||
chr11:46993884 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+6574C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993884 | |||||||
chr11:46993951 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+6641G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46993951 | |||||||
chr11:46994000 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+6690G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46994000 | |||||||
chr11:46994153 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+6843C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46994153 | |||||||
chr11:46994502 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149+7192T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46994502 | |||||||
chr11:46995146 | G | A | 54 | a0001c0001t0001g0064 a0001c0001t0001g0076 a0001c0001t0001g0077 others(51): Show |
54 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.149+7836G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995146 | |||||||
chr11:46995588 | T | TGA | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+8284_149+8285d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46995588 | ||||||
chr11:46995602 | C | A | 7 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0134 others(4): Show |
7 | HG00738.hp1 HG00741.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+8292C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995602 | |||||||
chr11:46995605 | G | C | 7 | a0001c0001t0001g0122 a0001c0001t0001g0130 a0001c0001t0001g0134 others(4): Show |
7 | HG00738.hp1 HG00741.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+8295G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995605 | |||||||
chr11:46995652 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.149+8342T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995652 | |||||||
chr11:46995778 | A | G | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.149+8468A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995778 | |||||||
chr11:46995960 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+8650C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995960 | |||||||
chr11:46995974 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.149+8664G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46995974 | |||||||
chr11:46996080 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.149+8770T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996080 | |||||||
chr11:46996088 | T | G | 1 | a0001c0001t0003g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.149+8778T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996088 | |||||||
chr11:46996244 | G | A | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.149+8934G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996244 | |||||||
chr11:46996310 | A | AT | 53 | a0001c0001t0001g0015 a0001c0001t0001g0019 a0001c0001t0001g0020 others(50): Show |
53 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.149+9011dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46996310 | ||||||
chr11:46996310 | AT | A | 57 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(54): Show |
57 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(54): Show |
intron_variant | MODIFIER | c.149+9011delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46996310 | ||||||
chr11:46996316 | T | A | 4 | a0001c0001t0001g0081 a0001c0001t0001g0194 a0001c0001t0001g0197 others(1): Show |
4 | HG02451.hp1 HG02818.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.149+9006T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996316 | |||||||
chr11:46996327 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+9017G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996327 | |||||||
chr11:46996397 | G | A | 1 | a0004c0006t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.149+9087G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996397 | |||||||
chr11:46996453 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.149+9143G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996453 | |||||||
chr11:46996538 | G | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.149+9228G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996538 | |||||||
chr11:46996545 | G | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.149+9235G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996545 | |||||||
chr11:46996829 | G | A | 1 | a0005c0008t0001g0003 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.149+9519G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996829 | |||||||
chr11:46996872 | G | A | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.149+9562G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996872 | |||||||
chr11:46996920 | A | G | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.149+9610A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996920 | |||||||
chr11:46996951 | C | T | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.149+9641C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46996951 | |||||||
chr11:46997240 | G | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.149+9930G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997240 | |||||||
chr11:46997254 | C | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+9944C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997254 | |||||||
chr11:46997424 | T | C | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+10114T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997424 | |||||||
chr11:46997844 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.149+10534T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997844 | |||||||
chr11:46997873 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+10563G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997873 | |||||||
chr11:46997909 | C | G | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.149+10599C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997909 | |||||||
chr11:46997971 | A | G | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+10661A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46997971 | |||||||
chr11:46998226 | G | C | 155 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(152): Show |
155 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(152): Show |
intron_variant | MODIFIER | c.149+10916G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998226 | |||||||
chr11:46998616 | A | G | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+11306A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998616 | |||||||
chr11:46998711 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.149+11401C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998711 | |||||||
chr11:46998925 | A | G | 1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.149+11615A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46998925 | |||||||
chr11:46999119 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.149+11809G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46999119 | |||||||
chr11:46999222 | AATAATAA others(4): Show |
A | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.149+11921_149+1193 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 46999222 | ||||||
chr11:46999663 | G | A | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+12353G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46999663 | |||||||
chr11:46999896 | G | A | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+12586G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 46999896 | |||||||
chr11:47000750 | GT | G | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+13441delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47000750 | |||||||
chr11:47001181 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149+13871T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47001181 | |||||||
chr11:47001399 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+14089T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47001399 | |||||||
chr11:47001476 | G | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+14166G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47001476 | |||||||
chr11:47002146 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.149+14836C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002146 | |||||||
chr11:47002254 | T | G | 1 | a0001c0001t0001g0152 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.149+14944T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002254 | |||||||
chr11:47002628 | C | G | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.149+15318C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002628 | |||||||
chr11:47002982 | T | A | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.149+15672T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47002982 | |||||||
chr11:47003502 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+16192C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47003502 | |||||||
chr11:47003560 | CTCAGGAT others(3): Show |
C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+16257_149+1626 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47003560 | ||||||
chr11:47003565 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+16255G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47003565 | |||||||
chr11:47003960 | C | G | 1 | a0001c0001t0001g0032 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.149+16650C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47003960 | |||||||
chr11:47004134 | TTTGTTG | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+16836_149+1684 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47004134 | ||||||
chr11:47004160 | GTTTTTGT others(7): Show |
G | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.149+16870_149+1688 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47004160 | ||||||
chr11:47004343 | CT | C | 53 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(50): Show |
53 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(50): Show |
intron_variant | MODIFIER | c.149+17043delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47004343 | ||||||
chr11:47004525 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.149+17215C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47004525 | |||||||
chr11:47005148 | AAG | A | 13 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0094 others(10): Show |
13 | HG00642.hp1 HG01081.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.149+17842_149+1784 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47005148 | ||||||
chr11:47006590 | CT | C | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | HG02451.hp1 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+19292delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006590 | ||||||
chr11:47006618 | T | C | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.149+19308T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47006618 | |||||||
chr11:47006746 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0143 a0001c0001t0001g0144 |
3 | HG02293.hp2 HG02300.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.149+19436A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47006746 | |||||||
chr11:47006755 | A | AT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(21): Show |
24 | HG00642.hp2 HG00735.hp2 HG01192.hp2 others(21): Show |
intron_variant | MODIFIER | c.149+19464dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006755 | ||||||
chr11:47006755 | A | ATT | 5 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0001t0001g0127 others(2): Show |
5 | HG01192.hp1 NA18960.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+19463_149+1946 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006755 | ||||||
chr11:47006755 | A | ATTT | 14 | a0001c0001t0001g0043 a0001c0001t0001g0084 a0001c0001t0001g0094 others(11): Show |
14 | HG00642.hp1 HG01081.hp1 HG01243.hp2 others(11): Show |
intron_variant | MODIFIER | c.149+19462_149+1946 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47006755 | ||||||
chr11:47006980 | C | T | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.149+19670C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47006980 | |||||||
chr11:47007001 | G | GT | 73 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0013 others(70): Show |
73 | HG00280.hp2 HG00438.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.149+19713dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47007001 | ||||||
chr11:47007001 | G | GTT | 7 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0081 others(4): Show |
7 | HG00438.hp1 HG02293.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+19712_149+1971 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47007001 | ||||||
chr11:47007748 | G | A | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.149+20438G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47007748 | |||||||
chr11:47008062 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+20752G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47008062 | |||||||
chr11:47009198 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+21888C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009198 | |||||||
chr11:47009551 | C | A | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+22241C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009551 | |||||||
chr11:47009886 | T | C | 1 | a0001c0001t0001g0152 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.149+22576T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009886 | |||||||
chr11:47009940 | A | G | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+22630A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009940 | |||||||
chr11:47009987 | A | G | 18 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0102 others(15): Show |
18 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.149+22677A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47009987 | |||||||
chr11:47010085 | G | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+22775G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47010085 | |||||||
chr11:47010387 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+23077C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47010387 | |||||||
chr11:47010499 | C | T | 1 | a0001c0001t0002g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.149+23189C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47010499 | |||||||
chr11:47011218 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+23908C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011218 | |||||||
chr11:47011234 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.149+23924T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011234 | |||||||
chr11:47011266 | T | C | 1 | a0001c0001t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.149+23956T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011266 | |||||||
chr11:47011320 | A | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+24010A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011320 | |||||||
chr11:47011343 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+24033G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011343 | |||||||
chr11:47011346 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.149+24036A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011346 | |||||||
chr11:47011373 | A | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+24063A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011373 | |||||||
chr11:47011572 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+24262T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011572 | |||||||
chr11:47011650 | T | G | 1 | a0001c0001t0001g0154 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.149+24340T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47011650 | |||||||
chr11:47012150 | A | G | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+24840A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47012150 | |||||||
chr11:47012528 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149+25218G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47012528 | |||||||
chr11:47012683 | C | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+25373C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47012683 | |||||||
chr11:47012995 | T | TTA | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.149+25695_149+2569 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47012995 | ||||||
chr11:47013000 | T | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+25690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47013000 | |||||||
chr11:47013006 | T | TA | 103 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(100): Show |
103 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.149+25696_149+2569 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47013006 | |||||||
chr11:47013131 | G | GCATATAT others(39): Show |
9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.149+25859_149+2590 others(50): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47013131 | ||||||
chr11:47013817 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+26507A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47013817 | |||||||
chr11:47014022 | A | G | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.149+26712A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014022 | |||||||
chr11:47014129 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.149+26819G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014129 | |||||||
chr11:47014183 | A | T | 1 | a0001c0001t0002g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.149+26873A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014183 | |||||||
chr11:47014210 | G | A | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.149+26900G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014210 | |||||||
chr11:47014308 | GAGAA | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0219 |
3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.149+27006_149+2700 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47014308 | ||||||
chr11:47014385 | GA | G | 76 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(73): Show |
76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.149+27085delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47014385 | ||||||
chr11:47014954 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.149+27644G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47014954 | |||||||
chr11:47015116 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.149+27806C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015116 | |||||||
chr11:47015243 | G | C | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.149+27933G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015243 | |||||||
chr11:47015304 | T | TA | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.149+28006dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47015304 | ||||||
chr11:47015399 | G | A | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+28089G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015399 | |||||||
chr11:47015499 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.149+28189A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015499 | |||||||
chr11:47015553 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+28243C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47015553 | |||||||
chr11:47016255 | G | A | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+28945G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016255 | |||||||
chr11:47016390 | C | CA | 6 | a0001c0001t0001g0013 a0001c0001t0001g0037 a0001c0001t0001g0090 others(3): Show |
6 | HG01243.hp2 HG01934.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.149+29086dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016390 | ||||||
chr11:47016390 | C | CAA | 10 | a0001c0001t0001g0084 a0001c0001t0001g0094 a0001c0001t0001g0107 others(7): Show |
10 | HG00642.hp1 HG01081.hp1 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+29085_149+2908 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016390 | ||||||
chr11:47016396 | AC | A | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG02572.hp2 HG02615.hp1 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.149+29087delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016396 | |||||||
chr11:47016397 | C | A | 205 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(202): Show |
205 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(202): Show |
intron_variant | MODIFIER | c.149+29087C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016397 | |||||||
chr11:47016399 | A | C | 121 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0082 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.149+29089A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016399 | |||||||
chr11:47016400 | A | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.149+29090A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016400 | |||||||
chr11:47016401 | A | C | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.149+29091A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016401 | |||||||
chr11:47016404 | C | A | 143 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(140): Show |
143 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.149+29094C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016404 | |||||||
chr11:47016410 | A | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.149+29100A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016410 | |||||||
chr11:47016411 | C | A | 3 | a0001c0001t0001g0081 a0001c0001t0001g0107 a0001c0001t0001g0121 |
3 | HG02145.hp1 HG02451.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.149+29101C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016411 | |||||||
chr11:47016421 | A | C | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.149+29111A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016421 | |||||||
chr11:47016515 | A | G | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.149+29205A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016515 | |||||||
chr11:47016526 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.149+29216G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016526 | |||||||
chr11:47016669 | A | G | 166 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(163): Show |
166 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(163): Show |
intron_variant | MODIFIER | c.149+29359A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016669 | |||||||
chr11:47016754 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.149+29444C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016754 | |||||||
chr11:47016808 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.149+29498C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016808 | |||||||
chr11:47016839 | C | CT | 102 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0043 others(99): Show |
102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.149+29550dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016839 | ||||||
chr11:47016839 | C | CTT | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | HG02257.hp2 HG02280.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+29549_149+2955 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47016839 | ||||||
chr11:47016877 | C | G | 1 | a0001c0001t0001g0042 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.149+29567C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016877 | |||||||
chr11:47016978 | A | G | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.149+29668A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47016978 | |||||||
chr11:47017009 | A | AT | 5 | a0001c0001t0001g0012 a0001c0001t0001g0186 a0001c0001t0001g0203 others(2): Show |
5 | HG01109.hp2 HG02257.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.149+29714dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017009 | ||||||
chr11:47017173 | AT | A | 142 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(139): Show |
142 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(139): Show |
intron_variant | MODIFIER | c.149+29882delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017173 | ||||||
chr11:47017203 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.149+29893C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017203 | |||||||
chr11:47017235 | C | T | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.149+29925C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017235 | |||||||
chr11:47017238 | A | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.149+29928A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017238 | |||||||
chr11:47017656 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.149+30346C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47017656 | |||||||
chr11:47017667 | CT | C | 26 | a0001c0001t0001g0048 a0001c0001t0001g0058 a0001c0001t0001g0071 others(23): Show |
26 | HG01192.hp2 HG01243.hp1 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.149+30375delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017667 | ||||||
chr11:47017667 | CTT | C | 87 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(84): Show |
87 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.149+30374_149+3037 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017667 | ||||||
chr11:47017667 | CTTT | C | 10 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
10 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.149+30373_149+3037 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47017667 | ||||||
chr11:47018287 | C | CT | 20 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0017 others(17): Show |
20 | HG00673.hp2 HG01934.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.149+31002dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47018287 | ||||||
chr11:47018287 | CT | C | 10 | a0001c0001t0001g0048 a0001c0001t0001g0061 a0001c0001t0001g0101 others(7): Show |
10 | HG00621.hp2 HG01081.hp1 HG01993.hp2 others(7): Show |
intron_variant | MODIFIER | c.149+31002delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47018287 | ||||||
chr11:47018460 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.149+31150A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018460 | |||||||
chr11:47018483 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.149+31173C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018483 | |||||||
chr11:47018528 | C | T | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+31218C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018528 | |||||||
chr11:47018561 | G | T | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.149+31251G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47018561 | |||||||
chr11:47019030 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.149+31720G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019030 | |||||||
chr11:47019153 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.149+31843G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019153 | |||||||
chr11:47019303 | A | G | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.149+31993A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019303 | |||||||
chr11:47019396 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.149+32086G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019396 | |||||||
chr11:47019514 | G | A | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.149+32204G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019514 | |||||||
chr11:47019612 | A | C | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.149+32302A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47019612 | |||||||
chr11:47020108 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.150-32280A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020108 | |||||||
chr11:47020340 | C | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-32048C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020340 | |||||||
chr11:47020604 | A | G | 1 | a0001c0001t0001g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.150-31784A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020604 | |||||||
chr11:47020605 | CTA | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-31781_150-3178 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47020605 | ||||||
chr11:47020949 | A | C | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.150-31439A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47020949 | |||||||
chr11:47021267 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-31121G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47021267 | |||||||
chr11:47021581 | G | A | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.150-30807G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47021581 | |||||||
chr11:47021682 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150-30706G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47021682 | |||||||
chr11:47021903 | CCCAATGA others(3): Show |
C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-30483_150-3047 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47021903 | ||||||
chr11:47022004 | G | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-30384G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022004 | |||||||
chr11:47022035 | G | GT | 8 | a0001c0001t0001g0013 a0001c0001t0001g0043 a0001c0001t0001g0044 others(5): Show |
8 | HG01261.hp1 HG01934.hp2 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-30338dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022035 | ||||||
chr11:47022155 | T | TAA | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-30231_150-3023 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022155 | ||||||
chr11:47022273 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.150-30115G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022273 | |||||||
chr11:47022312 | C | A | 5 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0132 others(2): Show |
5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-30076C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022312 | |||||||
chr11:47022358 | C | CT | 9 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0016 others(6): Show |
9 | HG00597.hp1 HG01934.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-30002dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022358 | ||||||
chr11:47022358 | CT | C | 48 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(45): Show |
48 | HG00597.hp2 HG00642.hp1 HG01071.hp1 others(45): Show |
intron_variant | MODIFIER | c.150-30002delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022358 | ||||||
chr11:47022358 | CTT | C | 99 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0089 others(96): Show |
99 | HG00280.hp2 HG00609.hp1 HG00621.hp2 others(96): Show |
intron_variant | MODIFIER | c.150-30003_150-3000 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022358 | ||||||
chr11:47022401 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-29987G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022401 | |||||||
chr11:47022420 | A | AGTACAGT | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-29966_150-2996 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47022420 | ||||||
chr11:47022489 | C | T | 5 | a0001c0001t0001g0012 a0001c0001t0001g0046 a0001c0001t0001g0054 others(2): Show |
5 | HG01074.hp1 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-29899C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022489 | |||||||
chr11:47022515 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.150-29873G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022515 | |||||||
chr11:47022552 | T | C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-29836T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022552 | |||||||
chr11:47022562 | G | T | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-29826G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022562 | |||||||
chr11:47022567 | A | G | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.150-29821A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022567 | |||||||
chr11:47022571 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.150-29817T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022571 | |||||||
chr11:47022623 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.150-29765G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022623 | |||||||
chr11:47022693 | T | C | 2 | a0001c0001t0001g0192 a0004c0006t0001g0200 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.150-29695T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022693 | |||||||
chr11:47022698 | T | C | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-29690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022698 | |||||||
chr11:47022804 | G | A | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-29584G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022804 | |||||||
chr11:47022813 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.150-29575C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47022813 | |||||||
chr11:47023220 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.150-29168G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47023220 | |||||||
chr11:47023528 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.150-28860C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47023528 | |||||||
chr11:47023816 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.150-28572G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47023816 | |||||||
chr11:47024303 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.150-28085A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47024303 | |||||||
chr11:47024378 | T | C | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-28010T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47024378 | |||||||
chr11:47024390 | A | G | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.150-27998A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47024390 | |||||||
chr11:47025003 | G | A | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.150-27385G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025003 | |||||||
chr11:47025505 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-26883A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025505 | |||||||
chr11:47025508 | A | G | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.150-26880A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025508 | |||||||
chr11:47025569 | G | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0151 |
2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150-26819G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025569 | |||||||
chr11:47025671 | T | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-26717T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025671 | |||||||
chr11:47025684 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.150-26704G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025684 | |||||||
chr11:47025859 | A | C | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.150-26529A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47025859 | |||||||
chr11:47026440 | AT | A | 4 | a0001c0001t0001g0053 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02723.hp2 HG03130.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-25939delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47026440 | ||||||
chr11:47026464 | T | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.150-25924T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47026464 | |||||||
chr11:47027149 | T | TA | 15 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(12): Show |
15 | HG00438.hp2 HG01361.hp2 HG01975.hp1 others(12): Show |
intron_variant | MODIFIER | c.150-25232dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47027149 | ||||||
chr11:47027684 | G | C | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.150-24704G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47027684 | |||||||
chr11:47027927 | C | CT | 130 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(127): Show |
130 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(127): Show |
intron_variant | MODIFIER | c.150-24447dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47027927 | ||||||
chr11:47028072 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.150-24316C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028072 | |||||||
chr11:47028108 | A | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0102 others(2): Show |
5 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-24280A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028108 | |||||||
chr11:47028109 | G | A | 2 | a0001c0001t0001g0091 a0001c0001t0001g0092 |
2 | HG01099.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.150-24279G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028109 | |||||||
chr11:47028649 | A | G | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-23739A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028649 | |||||||
chr11:47028671 | G | A | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.150-23717G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028671 | |||||||
chr11:47028759 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.150-23629T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028759 | |||||||
chr11:47028772 | CAA | C | 4 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-23614_150-2361 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47028772 | ||||||
chr11:47028846 | C | CT | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-23533dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47028846 | ||||||
chr11:47028983 | G | T | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.150-23405G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47028983 | |||||||
chr11:47029609 | C | CT | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-22778dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47029609 | ||||||
chr11:47029899 | A | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-22489A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47029899 | |||||||
chr11:47029923 | C | T | 2 | a0001c0001t0001g0130 a0001c0001t0001g0151 |
2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150-22465C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47029923 | |||||||
chr11:47029937 | G | GA | 24 | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0033 others(21): Show |
24 | HG00280.hp1 HG00438.hp1 HG00741.hp1 others(21): Show |
intron_variant | MODIFIER | c.150-22436dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47029937 | ||||||
chr11:47029937 | GA | G | 7 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0028 others(4): Show |
7 | HG00597.hp1 HG01081.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.150-22436delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47029937 | ||||||
chr11:47030522 | T | C | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-21866T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47030522 | |||||||
chr11:47030671 | C | T | 1 | a0001c0001t0001g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.150-21717C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47030671 | |||||||
chr11:47031478 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.150-20910G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47031478 | |||||||
chr11:47031696 | CT | C | 17 | a0001c0001t0001g0001 a0001c0001t0001g0045 a0001c0001t0001g0056 others(14): Show |
17 | HG00642.hp1 HG01515.hp1 HG01975.hp2 others(14): Show |
intron_variant | MODIFIER | c.150-20673delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47031696 | ||||||
chr11:47031698 | T | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-20690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47031698 | |||||||
chr11:47031715 | T | A | 134 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(131): Show |
134 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(131): Show |
intron_variant | MODIFIER | c.150-20673T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47031715 | |||||||
chr11:47032091 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-20297C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032091 | |||||||
chr11:47032349 | T | C | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-20039T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032349 | |||||||
chr11:47032531 | T | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-19857T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032531 | |||||||
chr11:47032559 | A | C | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.150-19829A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032559 | |||||||
chr11:47032637 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.150-19751C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032637 | |||||||
chr11:47032797 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.150-19591T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032797 | |||||||
chr11:47032816 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-19572A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032816 | |||||||
chr11:47032897 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-19491A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47032897 | |||||||
chr11:47033035 | T | G | 2 | a0001c0001t0001g0142 a0001c0001t0001g0157 |
2 | NA18955.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.150-19353T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47033035 | |||||||
chr11:47033229 | AT | A | 147 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(144): Show |
147 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(144): Show |
intron_variant | MODIFIER | c.150-19151delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47033229 | ||||||
chr11:47033963 | TA | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-18421delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47033963 | ||||||
chr11:47034049 | T | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-18339T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034049 | |||||||
chr11:47034153 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-18235C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034153 | |||||||
chr11:47034332 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-18056G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034332 | |||||||
chr11:47034504 | CT | C | 123 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(120): Show |
123 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.150-17869delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47034504 | ||||||
chr11:47034623 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-17765C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034623 | |||||||
chr11:47034632 | C | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-17756C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034632 | |||||||
chr11:47034901 | T | C | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-17487T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47034901 | |||||||
chr11:47035209 | A | T | 2 | a0001c0001t0001g0111 a0001c0001t0001g0170 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.150-17179A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035209 | |||||||
chr11:47035458 | T | A | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.150-16930T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035458 | |||||||
chr11:47035639 | C | A | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.150-16749C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035639 | |||||||
chr11:47035687 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.150-16701T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47035687 | |||||||
chr11:47036034 | G | GAT | 11 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0038 others(8): Show |
11 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-16333_150-1633 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | G | GATATATA others(5): Show |
2 | a0001c0001t0001g0128 a0001c0001t0003g0093 |
2 | HG01496.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.150-16343_150-1633 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | G | GATATATA others(7): Show |
3 | a0001c0001t0003g0097 a0001c0001t0003g0098 a0001c0001t0003g0100 |
3 | HG01192.hp1 HG02004.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.150-16345_150-1633 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | G | GATATATA others(9): Show |
2 | a0001c0001t0001g0084 a0001c0001t0001g0127 |
2 | NA18960.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.150-16347_150-1633 others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | G | GATATATA others(11): Show |
4 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0001t0001g0168 others(1): Show |
4 | HG01243.hp2 HG03579.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.150-16349_150-1633 others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | G | GATATATA others(13): Show |
2 | a0001c0001t0001g0121 a0001c0001t0003g0159 |
2 | HG01081.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1633 others(24): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | G | GATATATA others(15): Show |
1 | a0003c0002t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.150-16353_150-1633 others(26): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | GAT | G | 6 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0020 others(3): Show |
6 | HG01099.hp1 HG01993.hp1 HG02080.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-16333_150-1633 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036034 | GATATAT | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0094 |
2 | HG00280.hp1 HG00642.hp1 |
intron_variant | MODIFIER | c.150-16337_150-1633 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036034 | ||||||
chr11:47036036 | T | TAAAAGTG others(238): Show |
1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(249): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036036 | ||||||
chr11:47036036 | T | TAAAAGTG others(226): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(237): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036036 | ||||||
chr11:47036037 | A | AAAAGTGG others(276): Show |
1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(287): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(250): Show |
1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(261): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(255): Show |
15 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(12): Show |
15 | HG02451.hp2 HG02559.hp2 HG02622.hp2 others(12): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(266): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(224): Show |
3 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 |
3 | HG01243.hp1 HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(235): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(240): Show |
3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(251): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(229): Show |
2 | a0001c0001t0001g0193 a0004c0006t0001g0200 |
2 | HG02895.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(240): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(240): Show |
1 | a0001c0001t0002g0206 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(251): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(245): Show |
9 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(6): Show |
9 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(256): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(250): Show |
12 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0201 others(9): Show |
12 | HG01261.hp1 HG02109.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(261): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(330): Show |
1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(341): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(250): Show |
2 | a0001c0001t0001g0112 a0001c0004t0001g0113 |
2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.150-16351_150-1635 others(261): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(234): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0106 others(1): Show |
4 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(245): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(255): Show |
17 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0109 others(14): Show |
17 | HG00609.hp1 HG00621.hp2 HG02004.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(266): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(279): Show |
1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.150-16351_150-1635 others(290): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(253): Show |
1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(264): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(241): Show |
4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(252): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(284): Show |
1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-16351_150-1635 others(295): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | A | AAAAGTGG others(283): Show |
4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16351_150-1635 others(294): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036037 | ATATATAT others(6096): Show |
A | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-16350_150-1024 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036037 | |||||||
chr11:47036043 | A | AT | 73 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0101 others(70): Show |
73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16344dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036043 | ||||||
chr11:47036044 | T | TA | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16343dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036044 | ||||||
chr11:47036048 | TA | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0212 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16339delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036048 | |||||||
chr11:47036050 | TA | T | 72 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0103 others(69): Show |
72 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-16337delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036050 | |||||||
chr11:47036051 | A | AT | 10 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(7): Show |
10 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.150-16336dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036051 | ||||||
chr11:47036058 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-16330A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036058 | |||||||
chr11:47036060 | A | ATAT | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16327_150-1632 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036060 | ||||||
chr11:47036062 | A | AT | 2 | a0001c0001t0001g0081 a0001c0001t0001g0212 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16325dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036062 | ||||||
chr11:47036063 | TA | T | 73 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0103 others(70): Show |
73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16324delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036063 | |||||||
chr11:47036068 | A | T | 11 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(8): Show |
11 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(8): Show |
intron_variant | MODIFIER | c.150-16320A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036068 | |||||||
chr11:47036071 | A | AT | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16316dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036071 | ||||||
chr11:47036073 | A | AT | 72 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0103 others(69): Show |
72 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-16314dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036073 | ||||||
chr11:47036074 | T | TTATA | 2 | a0001c0001t0001g0081 a0001c0001t0001g0212 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16314_150-1631 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036074 | |||||||
chr11:47036076 | A | T | 85 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(82): Show |
85 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(82): Show |
intron_variant | MODIFIER | c.150-16312A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036076 | |||||||
chr11:47036078 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-16310T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036078 | |||||||
chr11:47036079 | T | A | 73 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0101 others(70): Show |
73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16309T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036079 | |||||||
chr11:47036080 | A | T | 2 | a0001c0001t0001g0081 a0001c0001t0001g0212 |
2 | HG02280.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.150-16308A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036080 | |||||||
chr11:47036081 | T | TA | 9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16306dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036081 | ||||||
chr11:47036084 | A | AT | 72 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0103 others(69): Show |
72 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(69): Show |
intron_variant | MODIFIER | c.150-16303dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036084 | ||||||
chr11:47036085 | T | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-16303T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036085 | |||||||
chr11:47036087 | T | A | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-16301T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036087 | |||||||
chr11:47036087 | T | TA | 73 | a0001c0001t0001g0076 a0001c0001t0001g0101 a0001c0001t0001g0103 others(70): Show |
73 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.150-16301_150-1630 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036087 | |||||||
chr11:47036092 | T | TAATATAT others(2): Show |
9 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(6): Show |
9 | HG00738.hp2 HG01099.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-16296_150-1629 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036092 | |||||||
chr11:47036100 | T | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.150-16288T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036100 | |||||||
chr11:47036140 | TATATA | T | 2 | a0001c0001t0001g0211 a0001c0001t0001g0214 |
2 | HG01261.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.150-16242_150-1623 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036140 | ||||||
chr11:47036177 | TA | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-16208delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036177 | ||||||
chr11:47036194 | T | TATATATT others(29): Show |
1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.150-16182_150-1614 others(40): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036194 | ||||||
chr11:47036212 | T | TTAATATA others(71): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-16104_150-1610 others(82): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036212 | ||||||
chr11:47036221 | AAT | A | 2 | a0001c0001t0001g0033 a0001c0005t0001g0083 |
2 | HG00280.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.150-16159_150-1615 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036221 | ||||||
chr11:47036225 | TATATA | T | 12 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(9): Show |
12 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.150-16157_150-1615 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036225 | ||||||
chr11:47036262 | AAT | A | 55 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0102 others(52): Show |
55 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.150-16117_150-1611 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47036262 | ||||||
chr11:47036533 | G | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-15855G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036533 | |||||||
chr11:47036903 | A | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-15485A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036903 | |||||||
chr11:47036948 | T | C | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-15440T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47036948 | |||||||
chr11:47037049 | C | G | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-15339C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037049 | |||||||
chr11:47037206 | T | TATATCAA others(5): Show |
79 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(76): Show |
79 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.150-15182_150-1518 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037206 | |||||||
chr11:47037392 | A | T | 9 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(6): Show |
9 | HG01081.hp1 HG01192.hp1 HG02004.hp2 others(6): Show |
intron_variant | MODIFIER | c.150-14996A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037392 | |||||||
chr11:47037392 | AT | A | 72 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0101 others(69): Show |
72 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(69): Show |
intron_variant | MODIFIER | c.150-14984delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47037392 | ||||||
chr11:47037395 | T | A | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(63): Show |
66 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.150-14993T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037395 | |||||||
chr11:47037396 | T | A | 47 | a0001c0001t0001g0076 a0001c0001t0001g0109 a0001c0001t0001g0123 others(44): Show |
47 | HG01109.hp1 HG01109.hp2 HG01243.hp1 others(44): Show |
intron_variant | MODIFIER | c.150-14992T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037396 | |||||||
chr11:47037398 | T | A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0221 others(4): Show |
7 | HG01074.hp2 HG02615.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-14990T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037398 | |||||||
chr11:47037539 | T | C | 1 | a0001c0001t0001g0055 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.150-14849T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037539 | |||||||
chr11:47037597 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14791C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037597 | |||||||
chr11:47037611 | G | C | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.150-14777G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037611 | |||||||
chr11:47037662 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14726G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037662 | |||||||
chr11:47037915 | T | C | 2 | a0003c0002t0001g0086 a0003c0002t0001g0087 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.150-14473T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037915 | |||||||
chr11:47037936 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.150-14452G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037936 | |||||||
chr11:47037972 | G | T | 2 | a0001c0001t0001g0036 a0001c0001t0001g0062 |
2 | HG03831.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.150-14416G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037972 | |||||||
chr11:47037986 | C | A | 79 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(76): Show |
79 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.150-14402C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47037986 | |||||||
chr11:47038071 | C | T | 29 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0102 others(26): Show |
29 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(26): Show |
intron_variant | MODIFIER | c.150-14317C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038071 | |||||||
chr11:47038090 | GCCGGGCG others(43): Show |
G | 30 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0102 others(27): Show |
30 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.150-14284_150-1423 others(54): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038090 | ||||||
chr11:47038094 | G | T | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.150-14294G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038094 | |||||||
chr11:47038106 | A | AC | 45 | a0001c0001t0001g0021 a0001c0001t0001g0072 a0001c0001t0001g0076 others(42): Show |
45 | HG01081.hp2 HG01109.hp1 HG01109.hp2 others(42): Show |
intron_variant | MODIFIER | c.150-14275dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038106 | ||||||
chr11:47038108 | C | T | 4 | a0001c0001t0003g0093 a0001c0001t0003g0097 a0001c0001t0003g0098 others(1): Show |
4 | HG01081.hp1 HG01496.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14280C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038108 | |||||||
chr11:47038139 | GC | G | 144 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(141): Show |
144 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(141): Show |
intron_variant | MODIFIER | c.150-14246delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038139 | ||||||
chr11:47038202 | ACTCCTCA others(168): Show |
A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.150-14157_150-1398 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038202 | ||||||
chr11:47038256 | T | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.150-14132T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038256 | |||||||
chr11:47038328 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.150-14060G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038328 | |||||||
chr11:47038345 | C | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.150-14043C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038345 | |||||||
chr11:47038358 | T | C | 78 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(75): Show |
78 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(75): Show |
intron_variant | MODIFIER | c.150-14030T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038358 | |||||||
chr11:47038366 | C | T | 5 | a0001c0001t0003g0093 a0001c0001t0003g0097 a0001c0001t0003g0098 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-14022C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038366 | |||||||
chr11:47038431 | T | C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-13957T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038431 | |||||||
chr11:47038464 | C | A | 1 | a0001c0001t0001g0046 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.150-13924C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038464 | |||||||
chr11:47038489 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-13899C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038489 | |||||||
chr11:47038564 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-13824G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038564 | |||||||
chr11:47038641 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.150-13747C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038641 | |||||||
chr11:47038674 | G | C | 5 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0202 others(2): Show |
5 | HG02109.hp1 HG02572.hp1 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-13714G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038674 | |||||||
chr11:47038757 | TGGGCGGA others(33): Show |
T | 1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.150-13603_150-1356 others(44): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47038757 | ||||||
chr11:47038790 | C | T | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.150-13598C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038790 | |||||||
chr11:47038791 | G | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.150-13597G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038791 | |||||||
chr11:47038797 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-13591C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038797 | |||||||
chr11:47038947 | C | G | 5 | a0001c0001t0003g0093 a0001c0001t0003g0097 a0001c0001t0003g0098 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.150-13441C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47038947 | |||||||
chr11:47039104 | G | C | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-13284G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039104 | |||||||
chr11:47039202 | G | C | 74 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0101 others(71): Show |
74 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(71): Show |
intron_variant | MODIFIER | c.150-13186G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039202 | |||||||
chr11:47039267 | G | T | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.150-13121G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039267 | |||||||
chr11:47039420 | A | G | 1 | a0001c0001t0001g0213 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.150-12968A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039420 | |||||||
chr11:47039443 | C | CAGAGGGA others(16): Show |
1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.150-12929_150-1290 others(27): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47039443 | ||||||
chr11:47039613 | C | G | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-12775C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039613 | |||||||
chr11:47039680 | T | C | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG02559.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.150-12708T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47039680 | |||||||
chr11:47040394 | G | T | 1 | a0001c0001t0001g0069 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.150-11994G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040394 | |||||||
chr11:47040422 | G | C | 2 | a0001c0001t0001g0192 a0004c0006t0001g0200 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.150-11966G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040422 | |||||||
chr11:47040543 | G | T | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.150-11845G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040543 | |||||||
chr11:47040557 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.150-11831G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040557 | |||||||
chr11:47040987 | A | G | 101 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(98): Show |
101 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.150-11401A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47040987 | |||||||
chr11:47041328 | C | T | 3 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0075 |
3 | NA18973.hp2 NA18978.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.150-11060C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041328 | |||||||
chr11:47041380 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.150-11008G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041380 | |||||||
chr11:47041551 | A | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.150-10837A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041551 | |||||||
chr11:47041603 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-10785C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47041603 | |||||||
chr11:47042043 | A | T | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.150-10345A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042043 | |||||||
chr11:47042050 | T | A | 35 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(32): Show |
35 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.150-10338T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042050 | |||||||
chr11:47042142 | C | A | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10246C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042142 | |||||||
chr11:47042147 | A | G | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10241A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042147 | |||||||
chr11:47042149 | C | A | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10239C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042149 | |||||||
chr11:47042151 | A | AGT | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10237_150-1023 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042151 | |||||||
chr11:47042152 | T | G | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10236T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042152 | |||||||
chr11:47042155 | T | A | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10233T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042155 | |||||||
chr11:47042160 | T | C | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-10228T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042160 | |||||||
chr11:47042179 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.150-10209G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042179 | |||||||
chr11:47042204 | A | G | 1 | a0001c0001t0003g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.150-10184A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042204 | |||||||
chr11:47042345 | G | GT | 7 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0033 others(4): Show |
7 | HG00280.hp1 HG01071.hp2 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-10027dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47042345 | ||||||
chr11:47042345 | GT | G | 101 | a0001c0001t0001g0036 a0001c0001t0001g0072 a0001c0001t0001g0076 others(98): Show |
101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.150-10027delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47042345 | ||||||
chr11:47042351 | T | G | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-10037T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042351 | |||||||
chr11:47042660 | TA | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-9720delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47042660 | ||||||
chr11:47042948 | A | G | 1 | a0001c0001t0001g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.150-9440A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47042948 | |||||||
chr11:47043106 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-9282C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043106 | |||||||
chr11:47043217 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.150-9171T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043217 | |||||||
chr11:47043521 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-8867G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043521 | |||||||
chr11:47043630 | A | T | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.150-8758A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043630 | |||||||
chr11:47043921 | C | G | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.150-8467C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043921 | |||||||
chr11:47043959 | A | G | 2 | a0001c0001t0001g0194 a0001c0001t0001g0198 |
2 | HG02818.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-8429A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47043959 | |||||||
chr11:47044144 | G | A | 1 | a0001c0001t0001g0049 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.150-8244G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044144 | |||||||
chr11:47044202 | T | A | 2 | a0001c0001t0001g0130 a0001c0001t0001g0151 |
2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.150-8186T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044202 | |||||||
chr11:47044253 | C | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.150-8135C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044253 | |||||||
chr11:47044276 | C | G | 1 | a0003c0002t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.150-8112C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044276 | |||||||
chr11:47044508 | A | G | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.150-7880A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044508 | |||||||
chr11:47044789 | G | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.150-7599G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044789 | |||||||
chr11:47044903 | T | C | 2 | a0001c0001t0001g0048 a0001c0001t0001g0051 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.150-7485T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47044903 | |||||||
chr11:47045329 | A | G | 1 | a0001c0001t0001g0099 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.150-7059A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045329 | |||||||
chr11:47045355 | CT | C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-7030delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47045355 | ||||||
chr11:47045380 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.150-7008T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045380 | |||||||
chr11:47045525 | GT | G | 8 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(5): Show |
8 | HG00621.hp2 HG02080.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.150-6861delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47045525 | ||||||
chr11:47045753 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.150-6635T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045753 | |||||||
chr11:47045933 | C | T | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.150-6455C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045933 | |||||||
chr11:47045960 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-6428T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47045960 | |||||||
chr11:47046129 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.150-6259G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046129 | |||||||
chr11:47046273 | C | A | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-6115C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046273 | |||||||
chr11:47046626 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.150-5762C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046626 | |||||||
chr11:47046660 | C | CT | 110 | a0001c0001t0001g0038 a0001c0001t0001g0043 a0001c0001t0001g0058 others(107): Show |
110 | HG00280.hp2 HG00597.hp2 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.150-5704dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | ||||||
chr11:47046660 | C | CTT | 13 | a0001c0001t0001g0061 a0001c0001t0001g0085 a0001c0001t0001g0120 others(10): Show |
13 | HG00438.hp1 HG00738.hp1 HG01109.hp1 others(10): Show |
intron_variant | MODIFIER | c.150-5705_150-5704d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | ||||||
chr11:47046660 | CT | C | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(27): Show |
30 | HG00735.hp2 HG01074.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.150-5704delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | ||||||
chr11:47046660 | CTT | C | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-5705_150-5704d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046660 | ||||||
chr11:47046666 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.150-5722T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046666 | |||||||
chr11:47046840 | A | G | 1 | a0001c0001t0001g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.150-5548A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046840 | |||||||
chr11:47046904 | C | CT | 18 | a0001c0001t0001g0062 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.150-5470dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47046904 | ||||||
chr11:47046906 | T | C | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-5482T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046906 | |||||||
chr11:47046927 | G | T | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-5461G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47046927 | |||||||
chr11:47047417 | GA | G | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-4969delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47047417 | ||||||
chr11:47047421 | C | G | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-4967C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47047421 | |||||||
chr11:47047741 | G | T | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.150-4647G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47047741 | |||||||
chr11:47047983 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.150-4405G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47047983 | |||||||
chr11:47048197 | G | A | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-4191G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47048197 | |||||||
chr11:47048527 | A | G | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.150-3861A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47048527 | |||||||
chr11:47048874 | G | C | 47 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(44): Show |
47 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.150-3514G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47048874 | |||||||
chr11:47049364 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-3024C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049364 | |||||||
chr11:47049494 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.150-2894T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049494 | |||||||
chr11:47049546 | G | C | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.150-2842G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049546 | |||||||
chr11:47049607 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-2781C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049607 | |||||||
chr11:47049962 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-2426C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47049962 | |||||||
chr11:47050164 | T | C | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.150-2224T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050164 | |||||||
chr11:47050346 | C | T | 156 | a0001c0001t0001g0010 a0001c0001t0001g0048 a0001c0001t0001g0049 others(153): Show |
156 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(153): Show |
intron_variant | MODIFIER | c.150-2042C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050346 | |||||||
chr11:47050349 | G | A | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.150-2039G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050349 | |||||||
chr11:47050498 | G | T | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.150-1890G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050498 | |||||||
chr11:47050791 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.150-1597G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47050791 | |||||||
chr11:47051104 | T | C | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-1284T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051104 | |||||||
chr11:47051162 | T | C | 16 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.150-1226T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051162 | |||||||
chr11:47051163 | C | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.150-1225C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051163 | |||||||
chr11:47051254 | G | T | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.150-1134G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051254 | |||||||
chr11:47051318 | G | A | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.150-1070G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051318 | |||||||
chr11:47051611 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.150-777T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47051611 | |||||||
chr11:47051691 | C | CT | 11 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0101 others(8): Show |
11 | HG01109.hp1 HG02109.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.150-679dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr11 | 47051691 | ||||||
chr11:47052275 | G | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0066 |
2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.150-113G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 2/8 | chr11 | 47052275 | |||||||
chr11:47052539 | T | TTTCC | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+44_280+47dupCC others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47052539 | ||||||
chr11:47052583 | CTCTCTCT others(9): Show |
C | 1 | a0001c0004t0001g0113 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.280+79_280+94delCT others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47052583 | ||||||
chr11:47052928 | T | C | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+410T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47052928 | |||||||
chr11:47053245 | T | A | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.280+727T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47053245 | |||||||
chr11:47053548 | G | A | 1 | a0001c0001t0002g0210 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.280+1030G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47053548 | |||||||
chr11:47053619 | C | CA | 8 | a0001c0001t0001g0112 a0001c0001t0001g0156 a0001c0001t0001g0189 others(5): Show |
8 | HG01071.hp1 HG01515.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+1116dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47053619 | ||||||
chr11:47053771 | G | A | 1 | a0001c0001t0001g0048 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.280+1253G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47053771 | |||||||
chr11:47053778 | C | CA | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.280+1267dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47053778 | ||||||
chr11:47053945 | AAAAC | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+1443_280+1446d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47053945 | ||||||
chr11:47054032 | G | A | 1 | a0003c0002t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.280+1514G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054032 | |||||||
chr11:47054208 | G | T | 1 | a0001c0001t0001g0142 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.280+1690G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054208 | |||||||
chr11:47054310 | C | CA | 38 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0029 others(35): Show |
38 | HG00438.hp2 HG00597.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.280+1815dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054310 | ||||||
chr11:47054310 | C | CAA | 11 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0175 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.280+1814_280+1815d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054310 | ||||||
chr11:47054310 | C | CAAA | 5 | a0001c0001t0001g0174 a0001c0001t0001g0177 a0001c0001t0001g0180 others(2): Show |
5 | HG02559.hp2 HG02622.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+1813_280+1815d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054310 | ||||||
chr11:47054593 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+2075A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054593 | |||||||
chr11:47054836 | A | G | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+2318A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47054836 | |||||||
chr11:47054928 | A | AT | 11 | a0001c0001t0001g0007 a0001c0001t0001g0009 a0001c0001t0001g0019 others(8): Show |
11 | HG00642.hp2 HG00673.hp2 HG00741.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+2439dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | ||||||
chr11:47054928 | A | ATT | 5 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0028 others(2): Show |
5 | NA18983.hp1 NA18992.hp2 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+2438_280+2439d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | ||||||
chr11:47054928 | AT | A | 30 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(27): Show |
30 | HG00735.hp1 HG01074.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.280+2439delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | ||||||
chr11:47054928 | ATT | A | 52 | a0001c0001t0001g0048 a0001c0001t0001g0072 a0001c0001t0001g0082 others(49): Show |
52 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.280+2438_280+2439d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | ||||||
chr11:47054928 | ATTT | A | 78 | a0001c0001t0001g0076 a0001c0001t0001g0090 a0001c0001t0001g0091 others(75): Show |
78 | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(75): Show |
intron_variant | MODIFIER | c.280+2437_280+2439d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47054928 | ||||||
chr11:47055003 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.280+2485C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055003 | |||||||
chr11:47055420 | C | G | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.280+2902C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055420 | |||||||
chr11:47055481 | A | G | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+2963A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055481 | |||||||
chr11:47055533 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+3015G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055533 | |||||||
chr11:47055593 | A | G | 1 | a0001c0001t0001g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.280+3075A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055593 | |||||||
chr11:47055695 | T | A | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+3177T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47055695 | |||||||
chr11:47056148 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.280+3630A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056148 | |||||||
chr11:47056286 | C | T | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+3768C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056286 | |||||||
chr11:47056407 | T | C | 3 | a0001c0001t0001g0120 a0001c0001t0001g0124 a0001c0001t0001g0126 |
3 | NA18949.hp1 NA18977.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.280+3889T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056407 | |||||||
chr11:47056436 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+3918G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47056436 | |||||||
chr11:47057318 | A | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+4800A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057318 | |||||||
chr11:47057408 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+4890A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057408 | |||||||
chr11:47057680 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.280+5162G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057680 | |||||||
chr11:47057684 | T | C | 2 | a0001c0001t0001g0030 a0001c0001t0001g0071 |
2 | NA18964.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.280+5166T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057684 | |||||||
chr11:47057876 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.280+5358C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057876 | |||||||
chr11:47057925 | C | T | 4 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+5407C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47057925 | |||||||
chr11:47058096 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+5578G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058096 | |||||||
chr11:47058143 | G | C | 1 | a0001c0001t0001g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.280+5625G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058143 | |||||||
chr11:47058636 | T | C | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.280+6118T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058636 | |||||||
chr11:47058800 | C | T | 1 | a0002c0003t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+6282C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058800 | |||||||
chr11:47058831 | G | A | 1 | a0001c0001t0001g0045 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.280+6313G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47058831 | |||||||
chr11:47059199 | T | G | 1 | a0001c0001t0001g0188 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.280+6681T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059199 | |||||||
chr11:47059559 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+7041G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059559 | |||||||
chr11:47059579 | G | T | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.280+7061G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059579 | |||||||
chr11:47059741 | T | C | 1 | a0002c0003t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+7223T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059741 | |||||||
chr11:47059919 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+7401C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059919 | |||||||
chr11:47059963 | G | T | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+7445G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47059963 | |||||||
chr11:47060181 | C | T | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.280+7663C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060181 | |||||||
chr11:47060258 | C | CT | 20 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0016 others(17): Show |
20 | HG00597.hp1 HG00642.hp2 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.280+7760dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47060258 | ||||||
chr11:47060258 | CT | C | 124 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0081 others(121): Show |
124 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.280+7760delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47060258 | ||||||
chr11:47060263 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+7745T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060263 | |||||||
chr11:47060484 | C | T | 2 | a0003c0002t0001g0086 a0003c0002t0001g0087 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.280+7966C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060484 | |||||||
chr11:47060571 | C | A | 148 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0077 others(145): Show |
148 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.280+8053C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060571 | |||||||
chr11:47060704 | G | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+8186G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060704 | |||||||
chr11:47060873 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.280+8355G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060873 | |||||||
chr11:47060913 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+8395C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47060913 | |||||||
chr11:47061280 | A | G | 5 | a0001c0001t0001g0108 a0001c0001t0001g0141 a0001c0001t0001g0146 others(2): Show |
5 | HG00733.hp2 HG00735.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+8762A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47061280 | |||||||
chr11:47061307 | T | C | 76 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(73): Show |
76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.280+8789T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47061307 | |||||||
chr11:47061831 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+9313T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47061831 | |||||||
chr11:47062510 | G | C | 127 | a0001c0001t0001g0073 a0001c0001t0001g0076 a0001c0001t0001g0077 others(124): Show |
127 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.280+9992G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062510 | |||||||
chr11:47062669 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.280+10151C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062669 | |||||||
chr11:47062813 | C | T | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+10295C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062813 | |||||||
chr11:47062835 | C | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+10317C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47062835 | |||||||
chr11:47063320 | A | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+10802A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063320 | |||||||
chr11:47063360 | T | G | 2 | a0001c0001t0001g0101 a0001c0001t0001g0103 |
2 | NA18973.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.280+10842T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063360 | |||||||
chr11:47063375 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+10857G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063375 | |||||||
chr11:47063561 | A | G | 1 | a0002c0003t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+11043A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063561 | |||||||
chr11:47063626 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+11108T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063626 | |||||||
chr11:47063638 | G | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0061 |
2 | HG01192.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.280+11120G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063638 | |||||||
chr11:47063758 | G | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+11240G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063758 | |||||||
chr11:47063806 | T | C | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.280+11288T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063806 | |||||||
chr11:47063916 | A | C | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.280+11398A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47063916 | |||||||
chr11:47064259 | T | TGTAG | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+11744_280+1174 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47064259 | ||||||
chr11:47064261 | T | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+11743T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47064261 | |||||||
chr11:47064872 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.280+12354G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47064872 | |||||||
chr11:47065117 | G | A | 5 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(2): Show |
5 | HG02451.hp1 HG02572.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+12599G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065117 | |||||||
chr11:47065315 | A | AT | 18 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+12807dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065315 | ||||||
chr11:47065412 | C | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280+12894C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065412 | |||||||
chr11:47065577 | C | G | 123 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0076 others(120): Show |
123 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.280+13059C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065577 | |||||||
chr11:47065616 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+13098C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065616 | |||||||
chr11:47065754 | A | T | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+13236A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065754 | |||||||
chr11:47065757 | T | A | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+13239T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065757 | |||||||
chr11:47065789 | G | T | 49 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(46): Show |
49 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(46): Show |
intron_variant | MODIFIER | c.280+13271G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065789 | |||||||
chr11:47065898 | C | A | 1 | a0001c0001t0001g0149 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.280+13380C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47065898 | |||||||
chr11:47065977 | T | TTG | 4 | a0001c0001t0001g0033 a0001c0001t0001g0056 a0001c0001t0001g0059 others(1): Show |
4 | HG00280.hp1 HG01071.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+13483_280+1348 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTG | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+13481_280+1348 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTG | 16 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 others(13): Show |
16 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.280+13479_280+1348 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(1): Show |
6 | a0001c0001t0001g0072 a0001c0001t0001g0081 a0001c0001t0001g0084 others(3): Show |
6 | HG02451.hp1 HG03654.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.280+13477_280+1348 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(3): Show |
10 | a0001c0001t0001g0077 a0001c0001t0001g0095 a0001c0001t0001g0120 others(7): Show |
10 | HG00597.hp2 HG00609.hp1 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+13475_280+1348 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(5): Show |
33 | a0001c0001t0001g0114 a0001c0001t0001g0118 a0001c0001t0001g0124 others(30): Show |
33 | HG00280.hp2 HG00733.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.280+13473_280+1348 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(7): Show |
57 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(54): Show |
57 | HG00438.hp1 HG00621.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.280+13471_280+1348 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(9): Show |
8 | a0001c0001t0001g0134 a0001c0001t0001g0138 a0001c0001t0001g0174 others(5): Show |
8 | HG00673.hp1 HG00741.hp2 HG02132.hp1 others(5): Show |
intron_variant | MODIFIER | c.280+13469_280+1348 others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(11): Show |
11 | a0001c0001t0001g0172 a0001c0001t0001g0175 a0001c0001t0001g0176 others(8): Show |
11 | HG01243.hp1 HG01884.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+13467_280+1348 others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(13): Show |
2 | a0001c0001t0001g0152 a0001c0001t0001g0194 |
2 | HG03579.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.280+13465_280+1348 others(24): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47065977 | T | TTGTGTGT others(15): Show |
1 | a0001c0001t0001g0182 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.280+13463_280+1348 others(26): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47065977 | ||||||
chr11:47066093 | G | GGTT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+13575_280+1357 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066093 | |||||||
chr11:47066099 | T | TTTG | 127 | a0001c0001t0001g0072 a0001c0001t0001g0077 a0001c0001t0001g0078 others(124): Show |
127 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.280+13583_280+1358 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47066099 | ||||||
chr11:47066102 | T | G | 20 | a0001c0001t0001g0076 a0001c0001t0001g0110 a0001c0001t0001g0142 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+13584T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066102 | |||||||
chr11:47066102 | T | TG | 3 | a0001c0001t0001g0039 a0001c0001t0001g0042 a0001c0001t0001g0045 |
3 | HG01361.hp2 HG01975.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.280+13584_280+1358 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066102 | |||||||
chr11:47066109 | T | G | 4 | a0001c0001t0001g0104 a0001c0001t0001g0144 a0001c0001t0001g0154 others(1): Show |
4 | HG00735.hp1 HG01496.hp2 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.280+13591T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066109 | |||||||
chr11:47066112 | T | G | 128 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0077 others(125): Show |
128 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.280+13594T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066112 | |||||||
chr11:47066115 | T | TG | 40 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(37): Show |
40 | HG00597.hp1 HG00642.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.280+13597_280+1359 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066115 | |||||||
chr11:47066115 | T | TGTTG | 20 | a0001c0001t0001g0076 a0001c0001t0001g0110 a0001c0001t0001g0142 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG02004.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+13597_280+1359 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066115 | |||||||
chr11:47066115 | T | TTG | 11 | a0001c0001t0001g0001 a0001c0001t0001g0033 a0001c0001t0001g0041 others(8): Show |
11 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+13598_280+1359 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47066115 | ||||||
chr11:47066610 | A | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+14092A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066610 | |||||||
chr11:47066747 | G | A | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.280+14229G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066747 | |||||||
chr11:47066752 | T | C | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.280+14234T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066752 | |||||||
chr11:47066819 | G | T | 1 | a0001c0001t0001g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.280+14301G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47066819 | |||||||
chr11:47067199 | G | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.280+14681G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067199 | |||||||
chr11:47067330 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+14812A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067330 | |||||||
chr11:47067416 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+14898C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067416 | |||||||
chr11:47067830 | G | A | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.280+15312G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067830 | |||||||
chr11:47067930 | G | A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.280+15412G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47067930 | |||||||
chr11:47068100 | C | T | 1 | a0001c0001t0001g0071 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.280+15582C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068100 | |||||||
chr11:47068139 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+15621C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068139 | |||||||
chr11:47068361 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.280+15843G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068361 | |||||||
chr11:47068783 | A | G | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+16265A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068783 | |||||||
chr11:47068867 | A | C | 10 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
10 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+16349A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47068867 | |||||||
chr11:47069291 | C | T | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+16773C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47069291 | |||||||
chr11:47069716 | A | T | 13 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(10): Show |
13 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.280+17198A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47069716 | |||||||
chr11:47069719 | T | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+17201T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47069719 | |||||||
chr11:47070004 | C | T | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+17486C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070004 | |||||||
chr11:47070020 | C | T | 126 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(123): Show |
126 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.280+17502C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070020 | |||||||
chr11:47070387 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+17869C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070387 | |||||||
chr11:47070484 | A | T | 1 | a0001c0001t0001g0081 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.280+17966A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47070484 | |||||||
chr11:47071131 | C | T | 18 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+18613C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071131 | |||||||
chr11:47071152 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+18634G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071152 | |||||||
chr11:47071533 | T | C | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.280+19015T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071533 | |||||||
chr11:47071666 | C | CA | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+19150dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47071666 | ||||||
chr11:47071914 | C | G | 74 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(71): Show |
74 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.280+19396C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47071914 | |||||||
chr11:47072012 | C | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+19494C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072012 | |||||||
chr11:47072089 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.280+19571T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072089 | |||||||
chr11:47072717 | C | CTTATG | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.280+20203_280+2020 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47072717 | ||||||
chr11:47072742 | C | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0170 |
2 | HG02109.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.280+20224C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072742 | |||||||
chr11:47072925 | T | C | 1 | a0001c0001t0002g0205 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.280+20407T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072925 | |||||||
chr11:47072935 | A | C | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.280+20417A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072935 | |||||||
chr11:47072959 | A | G | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+20441A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072959 | |||||||
chr11:47072995 | G | A | 15 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(12): Show |
15 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.280+20477G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47072995 | |||||||
chr11:47073505 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.280+20987G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47073505 | |||||||
chr11:47073943 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+21425G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47073943 | |||||||
chr11:47073960 | G | C | 75 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(72): Show |
75 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(72): Show |
intron_variant | MODIFIER | c.280+21442G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47073960 | |||||||
chr11:47074501 | GAAAAA | G | 17 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0106 others(14): Show |
17 | HG00609.hp1 HG00738.hp1 HG00738.hp2 others(14): Show |
intron_variant | MODIFIER | c.280+21999_280+2200 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47074501 | ||||||
chr11:47074501 | GAAAAAA | G | 54 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(51): Show |
54 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(51): Show |
intron_variant | MODIFIER | c.280+21998_280+2200 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47074501 | ||||||
chr11:47074501 | GAAAAAAA others(3): Show |
G | 23 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(20): Show |
23 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.280+21994_280+2200 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47074501 | ||||||
chr11:47074512 | A | C | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+21994A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074512 | |||||||
chr11:47074514 | A | G | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+21996A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074514 | |||||||
chr11:47074515 | A | AC | 21 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0173 others(18): Show |
21 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.280+21997_280+2199 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074515 | |||||||
chr11:47074515 | A | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.280+21997A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074515 | |||||||
chr11:47074516 | A | C | 1 | a0001c0001t0001g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+21998A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074516 | |||||||
chr11:47074518 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+22000A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074518 | |||||||
chr11:47074855 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+22337C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074855 | |||||||
chr11:47074870 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+22352G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074870 | |||||||
chr11:47074879 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.280+22361A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074879 | |||||||
chr11:47074885 | T | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.280+22367T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074885 | |||||||
chr11:47074982 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.280+22464G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47074982 | |||||||
chr11:47075292 | AC | A | 101 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(98): Show |
101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.280+22777delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47075292 | ||||||
chr11:47075329 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+22811G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075329 | |||||||
chr11:47075430 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.280+22912G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075430 | |||||||
chr11:47075508 | A | G | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+22990A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075508 | |||||||
chr11:47075509 | T | C | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.280+22991T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075509 | |||||||
chr11:47075603 | G | C | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+23085G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075603 | |||||||
chr11:47075713 | G | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+23195G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075713 | |||||||
chr11:47075733 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+23215G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075733 | |||||||
chr11:47075747 | C | T | 18 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(15): Show |
18 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+23229C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075747 | |||||||
chr11:47075813 | G | T | 101 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(98): Show |
101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.280+23295G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47075813 | |||||||
chr11:47075926 | C | CA | 24 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0028 others(21): Show |
24 | HG00438.hp2 HG00642.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.280+23434dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47075926 | ||||||
chr11:47075926 | CA | C | 66 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0001c0001t0001g0082 others(63): Show |
66 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(63): Show |
intron_variant | MODIFIER | c.280+23434delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47075926 | ||||||
chr11:47076374 | C | G | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+23856C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076374 | |||||||
chr11:47076602 | A | T | 2 | a0001c0001t0001g0121 a0001c0001t0001g0168 |
2 | HG02145.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.280+24084A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076602 | |||||||
chr11:47076726 | C | T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(7): Show |
10 | HG00642.hp2 HG00733.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+24208C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076726 | |||||||
chr11:47076894 | A | C | 120 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(117): Show |
120 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.280+24376A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076894 | |||||||
chr11:47076918 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.280+24400G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47076918 | |||||||
chr11:47076963 | GA | G | 214 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(211): Show |
214 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(211): Show |
intron_variant | MODIFIER | c.280+24460delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47076963 | ||||||
chr11:47077196 | GT | G | 103 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(100): Show |
103 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(100): Show |
intron_variant | MODIFIER | c.280+24693delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47077196 | ||||||
chr11:47077269 | G | T | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+24751G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077269 | |||||||
chr11:47077333 | G | C | 5 | a0001c0001t0003g0093 a0001c0001t0003g0097 a0001c0001t0003g0098 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+24815G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077333 | |||||||
chr11:47077384 | A | G | 2 | a0001c0001t0002g0205 a0001c0001t0002g0218 |
2 | HG01884.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.280+24866A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077384 | |||||||
chr11:47077574 | A | C | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(65): Show |
68 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(65): Show |
intron_variant | MODIFIER | c.280+25056A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077574 | |||||||
chr11:47077616 | T | G | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+25098T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47077616 | |||||||
chr11:47078191 | A | G | 2 | a0001c0001t0001g0172 a0001c0001t0001g0178 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.280+25673A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078191 | |||||||
chr11:47078208 | T | C | 2 | a0001c0001t0001g0138 a0001c0001t0001g0160 |
2 | HG00597.hp2 HG02132.hp1 |
intron_variant | MODIFIER | c.280+25690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078208 | |||||||
chr11:47078218 | T | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+25700T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078218 | |||||||
chr11:47078298 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.280+25780G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078298 | |||||||
chr11:47078316 | C | T | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.280+25798C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078316 | |||||||
chr11:47078595 | T | C | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.280+26077T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47078595 | |||||||
chr11:47079245 | G | T | 76 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(73): Show |
76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.280+26727G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47079245 | |||||||
chr11:47079948 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.280+27430T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47079948 | |||||||
chr11:47080363 | G | T | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.280+27845G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080363 | |||||||
chr11:47080523 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.280+28005A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080523 | |||||||
chr11:47080632 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0170 others(1): Show |
4 | HG01071.hp1 HG01515.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+28114G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080632 | |||||||
chr11:47080896 | C | G | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+28378C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47080896 | |||||||
chr11:47081008 | CA | C | 20 | a0001c0001t0001g0017 a0001c0001t0001g0025 a0001c0001t0001g0027 others(17): Show |
20 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.280+28506delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47081008 | ||||||
chr11:47081103 | G | A | 1 | a0001c0001t0003g0100 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.280+28585G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47081103 | |||||||
chr11:47081935 | C | CT | 11 | a0001c0001t0001g0056 a0001c0001t0001g0106 a0001c0001t0001g0114 others(8): Show |
11 | HG00738.hp2 HG01243.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.280+29435dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47081935 | ||||||
chr11:47081935 | CT | C | 9 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(6): Show |
9 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.280+29435delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47081935 | ||||||
chr11:47082142 | C | A | 1 | a0001c0001t0001g0007 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.280+29624C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082142 | |||||||
chr11:47082149 | C | CA | 33 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(30): Show |
33 | HG00673.hp1 HG00733.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.280+29649dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082149 | ||||||
chr11:47082149 | C | CAA | 43 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(40): Show |
43 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.280+29648_280+2964 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082149 | ||||||
chr11:47082149 | C | CAAA | 14 | a0001c0001t0001g0011 a0001c0001t0001g0038 a0001c0001t0001g0039 others(11): Show |
14 | HG00438.hp2 HG01192.hp2 HG01361.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+29647_280+2964 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082149 | ||||||
chr11:47082257 | A | T | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+29739A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082257 | |||||||
chr11:47082326 | C | T | 16 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0106 others(13): Show |
16 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.280+29808C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082326 | |||||||
chr11:47082490 | C | CAG | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+29975_280+2997 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47082490 | ||||||
chr11:47082848 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+30330T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47082848 | |||||||
chr11:47083390 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.280+30872C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083390 | |||||||
chr11:47083610 | T | TA | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+31093dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47083610 | ||||||
chr11:47083701 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+31183G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083701 | |||||||
chr11:47083769 | G | C | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+31251G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083769 | |||||||
chr11:47083906 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0046 |
2 | HG03688.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.280+31388A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47083906 | |||||||
chr11:47084180 | C | G | 1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.280+31662C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084180 | |||||||
chr11:47084312 | A | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+31794A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084312 | |||||||
chr11:47084379 | T | C | 1 | a0001c0001t0001g0044 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.280+31861T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084379 | |||||||
chr11:47084763 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+32245G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084763 | |||||||
chr11:47084979 | G | A | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.280+32461G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47084979 | |||||||
chr11:47085129 | G | A | 1 | a0001c0001t0003g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.280+32611G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085129 | |||||||
chr11:47085443 | G | A | 17 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(14): Show |
17 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.280+32925G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085443 | |||||||
chr11:47085458 | T | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(2): Show |
5 | HG02615.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+32940T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085458 | |||||||
chr11:47085718 | C | T | 5 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0046 others(2): Show |
5 | HG01074.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.280+33200C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085718 | |||||||
chr11:47085863 | G | C | 1 | a0002c0003t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.280+33345G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085863 | |||||||
chr11:47085870 | T | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.280+33352T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085870 | |||||||
chr11:47085985 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.280+33467G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47085985 | |||||||
chr11:47086113 | G | T | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.280+33595G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086113 | |||||||
chr11:47086232 | T | TA | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(45): Show |
48 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.280+33714_280+3371 others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086232 | |||||||
chr11:47086232 | TCCAAAAA others(1): Show |
T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+33715_280+3372 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086232 | |||||||
chr11:47086233 | C | A | 163 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(160): Show |
163 | HG00280.hp2 HG00438.hp1 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.280+33715C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086233 | |||||||
chr11:47086234 | C | A | 48 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0007 others(45): Show |
48 | HG00280.hp1 HG00438.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.280+33716C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086234 | |||||||
chr11:47086234 | C | CAA | 34 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(31): Show |
34 | HG00597.hp1 HG00642.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.280+33738_280+3373 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | ||||||
chr11:47086234 | C | CAAA | 39 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0042 others(36): Show |
39 | HG00738.hp1 HG01109.hp2 HG01261.hp1 others(36): Show |
intron_variant | MODIFIER | c.280+33737_280+3373 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | ||||||
chr11:47086234 | C | CAAAA | 76 | a0001c0001t0001g0073 a0001c0001t0001g0082 a0001c0001t0001g0085 others(73): Show |
76 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.280+33736_280+3373 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | ||||||
chr11:47086234 | C | CAAAAA | 12 | a0001c0001t0001g0095 a0001c0001t0001g0102 a0001c0001t0001g0103 others(9): Show |
12 | HG00280.hp2 HG00597.hp2 HG00735.hp1 others(9): Show |
intron_variant | MODIFIER | c.280+33735_280+3373 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47086234 | ||||||
chr11:47086237 | A | C | 2 | a0001c0001t0001g0174 a0001c0001t0001g0180 |
2 | HG02559.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.280+33719A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086237 | |||||||
chr11:47086238 | A | C | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.280+33720A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086238 | |||||||
chr11:47086239 | A | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+33721A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086239 | |||||||
chr11:47086240 | A | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0143 |
2 | HG02293.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.280+33722A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086240 | |||||||
chr11:47086242 | A | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+33724A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086242 | |||||||
chr11:47086340 | C | T | 1 | a0001c0001t0001g0089 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.280+33822C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086340 | |||||||
chr11:47086618 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.280+34100A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086618 | |||||||
chr11:47086650 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.280+34132T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47086650 | |||||||
chr11:47087259 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.280+34741A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087259 | |||||||
chr11:47087261 | G | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+34743G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087261 | |||||||
chr11:47087304 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.280+34786T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087304 | |||||||
chr11:47087509 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.280+34991A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087509 | |||||||
chr11:47087706 | A | T | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+35188A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087706 | |||||||
chr11:47087717 | A | ATG | 5 | a0001c0001t0001g0096 a0001c0001t0001g0174 a0001c0001t0001g0180 others(2): Show |
5 | HG02257.hp1 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+35218_280+3521 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47087717 | ||||||
chr11:47087780 | C | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+35262C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087780 | |||||||
chr11:47087792 | A | G | 8 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0202 others(5): Show |
8 | HG02109.hp1 HG02572.hp1 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.280+35274A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087792 | |||||||
chr11:47087912 | T | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.280+35394T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087912 | |||||||
chr11:47087963 | G | C | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.280+35445G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47087963 | |||||||
chr11:47088257 | G | C | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.280+35739G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088257 | |||||||
chr11:47088273 | A | G | 1 | a0001c0001t0001g0124 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.280+35755A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088273 | |||||||
chr11:47088628 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.280+36110C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088628 | |||||||
chr11:47088798 | G | A | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.280+36280G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088798 | |||||||
chr11:47088995 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+36477T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47088995 | |||||||
chr11:47089041 | C | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+36523C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089041 | |||||||
chr11:47089058 | A | G | 1 | a0001c0001t0001g0166 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.280+36540A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089058 | |||||||
chr11:47089096 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+36578G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089096 | |||||||
chr11:47089101 | A | C | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.280+36583A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089101 | |||||||
chr11:47089435 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+36917A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47089435 | |||||||
chr11:47090067 | T | G | 1 | a0001c0001t0001g0037 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.280+37549T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090067 | |||||||
chr11:47090255 | G | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+37737G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090255 | |||||||
chr11:47090310 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.280+37792T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090310 | |||||||
chr11:47090467 | GA | G | 10 | a0001c0001t0002g0196 a0001c0001t0002g0199 a0001c0001t0002g0205 others(7): Show |
10 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.280+37958delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47090467 | ||||||
chr11:47090843 | T | C | 1 | a0001c0001t0001g0058 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.280+38325T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090843 | |||||||
chr11:47090901 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+38383C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47090901 | |||||||
chr11:47091046 | CA | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(131): Show |
134 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(131): Show |
intron_variant | MODIFIER | c.280+38547delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47091046 | ||||||
chr11:47091046 | CAA | C | 80 | a0001c0001t0001g0040 a0001c0001t0001g0043 a0001c0001t0001g0068 others(77): Show |
80 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(77): Show |
intron_variant | MODIFIER | c.280+38546_280+3854 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47091046 | ||||||
chr11:47091113 | T | C | 1 | a0001c0001t0003g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.280+38595T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091113 | |||||||
chr11:47091336 | T | C | 1 | a0001c0001t0001g0212 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.280+38818T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091336 | |||||||
chr11:47091373 | C | CA | 14 | a0001c0001t0001g0121 a0001c0001t0001g0192 a0001c0001t0001g0211 others(11): Show |
14 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.280+38869dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47091373 | ||||||
chr11:47091522 | G | T | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.280+39004G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091522 | |||||||
chr11:47091752 | C | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+39234C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47091752 | |||||||
chr11:47092455 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+39937T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092455 | |||||||
chr11:47092523 | C | T | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.280+40005C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092523 | |||||||
chr11:47092577 | A | T | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.280+40059A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092577 | |||||||
chr11:47092788 | A | G | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.280+40270A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092788 | |||||||
chr11:47092937 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.280+40419C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47092937 | |||||||
chr11:47093232 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.280+40714G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093232 | |||||||
chr11:47093273 | G | A | 13 | a0001c0001t0001g0089 a0001c0001t0001g0096 a0001c0001t0001g0104 others(10): Show |
13 | HG00597.hp2 HG00673.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.280+40755G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093273 | |||||||
chr11:47093487 | C | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+40969C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093487 | |||||||
chr11:47093720 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.280+41202G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093720 | |||||||
chr11:47093906 | C | T | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+41388C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47093906 | |||||||
chr11:47094002 | G | C | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.280+41484G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094002 | |||||||
chr11:47094168 | G | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.280+41650G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094168 | |||||||
chr11:47094206 | C | T | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.280+41688C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094206 | |||||||
chr11:47094217 | A | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(2): Show |
5 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(2): Show |
intron_variant | MODIFIER | c.280+41699A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094217 | |||||||
chr11:47094416 | C | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.280+41898C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094416 | |||||||
chr11:47094422 | T | G | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.280+41904T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094422 | |||||||
chr11:47094464 | T | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+41946T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094464 | |||||||
chr11:47094480 | C | CAG | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(68): Show |
71 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.280+41984_280+4198 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47094480 | ||||||
chr11:47094482 | G | C | 102 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(99): Show |
102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.280+41964G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094482 | |||||||
chr11:47094545 | C | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.280+42027C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094545 | |||||||
chr11:47094698 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.280+42180G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094698 | |||||||
chr11:47094950 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.280+42432A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47094950 | |||||||
chr11:47095272 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-42373T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47095272 | |||||||
chr11:47095581 | A | C | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-42064A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47095581 | |||||||
chr11:47095718 | G | A | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0219 |
3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.281-41927G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47095718 | |||||||
chr11:47095856 | A | AT | 6 | a0001c0001t0002g0199 a0001c0001t0002g0205 a0001c0001t0002g0207 others(3): Show |
6 | HG01109.hp2 HG01884.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-41781dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47095856 | ||||||
chr11:47096157 | T | C | 4 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0070 others(1): Show |
4 | NA18951.hp1 NA18971.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-41488T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47096157 | |||||||
chr11:47096576 | C | T | 1 | a0001c0001t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281-41069C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47096576 | |||||||
chr11:47096811 | G | GA | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(92): Show |
95 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.281-40818dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47096811 | ||||||
chr11:47097065 | C | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.281-40580C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097065 | |||||||
chr11:47097067 | C | G | 1 | a0003c0002t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.281-40578C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097067 | |||||||
chr11:47097071 | CGGCCAGC others(42): Show |
C | 1 | a0001c0001t0001g0055 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.281-40545_281-4049 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097071 | ||||||
chr11:47097120 | T | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-40525T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097120 | |||||||
chr11:47097121 | G | A | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-40524G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097121 | |||||||
chr11:47097154 | T | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-40491T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097154 | |||||||
chr11:47097162 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-40483C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097162 | |||||||
chr11:47097211 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(54): Show |
57 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.281-40434A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097211 | |||||||
chr11:47097243 | TGCCCGGC others(348): Show |
T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-40360_281-4000 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097243 | ||||||
chr11:47097248 | GGCCAGCC others(42): Show |
G | 5 | a0001c0001t0001g0002 a0001c0001t0001g0012 a0001c0001t0001g0046 others(2): Show |
5 | HG01074.hp2 HG01261.hp2 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-40355_281-4030 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097248 | ||||||
chr11:47097285 | A | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-40360A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097285 | |||||||
chr11:47097290 | C | A | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-40355C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097290 | |||||||
chr11:47097292 | CGCCCAGC others(120): Show |
C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.281-40348_281-4022 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097292 | ||||||
chr11:47097297 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0056 |
2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.281-40348A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097297 | |||||||
chr11:47097324 | TGGGGGGG others(119): Show |
T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0056 |
2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.281-40320_281-4019 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097324 | |||||||
chr11:47097342 | G | A | 2 | a0001c0001t0001g0092 a0001c0001t0001g0131 |
2 | HG03710.hp2 NA18989.hp2 |
intron_variant | MODIFIER | c.281-40303G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097342 | |||||||
chr11:47097362 | TGGGAGGT others(123): Show |
T | 17 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(14): Show |
17 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(14): Show |
intron_variant | MODIFIER | c.281-40186_281-4005 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097362 | ||||||
chr11:47097419 | T | TGCCCGGC others(42): Show |
106 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(103): Show |
106 | HG00280.hp2 HG00438.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.281-40187_281-4018 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097419 | ||||||
chr11:47097419 | T | TGCCCGGC others(270): Show |
1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.281-40187_281-4018 others(281): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097419 | ||||||
chr11:47097419 | TGCCCGGC others(172): Show |
T | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-40186_281-4000 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097419 | ||||||
chr11:47097451 | T | C | 2 | a0001c0001t0001g0013 a0001c0001t0001g0056 |
2 | HG01934.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.281-40194T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097451 | |||||||
chr11:47097451 | T | TGGGGGGG others(43): Show |
1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.281-40187_281-4018 others(54): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097451 | ||||||
chr11:47097451 | T | TGGGGGGG others(43): Show |
11 | a0001c0001t0001g0114 a0001c0001t0001g0135 a0001c0001t0001g0148 others(8): Show |
11 | HG00597.hp2 HG00735.hp1 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-40187_281-4018 others(54): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097451 | ||||||
chr11:47097452 | G | C | 53 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(50): Show |
53 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.281-40193G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097452 | |||||||
chr11:47097452 | G | GGGGGGGT others(41): Show |
1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.281-40187_281-4018 others(52): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097452 | ||||||
chr11:47097452 | G | GGGGGGGT others(42): Show |
21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(18): Show |
21 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(18): Show |
intron_variant | MODIFIER | c.281-40187_281-4018 others(53): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097452 | ||||||
chr11:47097468 | CCCTGCCC others(121): Show |
C | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-40174_281-4004 others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097468 | ||||||
chr11:47097493 | G | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-40152G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097493 | |||||||
chr11:47097596 | T | C | 218 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(215): Show |
218 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(215): Show |
intron_variant | MODIFIER | c.281-40049T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097596 | |||||||
chr11:47097612 | C | A | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.281-40033C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097612 | |||||||
chr11:47097640 | G | A | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-40005G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097640 | |||||||
chr11:47097679 | TG | T | 101 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(98): Show |
101 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(98): Show |
intron_variant | MODIFIER | c.281-39957delG | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47097679 | ||||||
chr11:47097684 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-39961G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097684 | |||||||
chr11:47097690 | C | T | 5 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0149 others(2): Show |
5 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-39955C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097690 | |||||||
chr11:47097710 | C | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-39935C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097710 | |||||||
chr11:47097748 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-39897C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097748 | |||||||
chr11:47097762 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281-39883A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097762 | |||||||
chr11:47097867 | C | A | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.281-39778C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47097867 | |||||||
chr11:47098253 | C | T | 1 | a0001c0001t0001g0144 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.281-39392C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098253 | |||||||
chr11:47098324 | A | T | 122 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(119): Show |
122 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.281-39321A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098324 | |||||||
chr11:47098504 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-39141T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098504 | |||||||
chr11:47098507 | CT | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-39123delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47098507 | ||||||
chr11:47098512 | T | C | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-39133T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098512 | |||||||
chr11:47098515 | T | C | 10 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0012 others(7): Show |
10 | HG00735.hp2 HG01074.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-39130T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098515 | |||||||
chr11:47098748 | C | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-38897C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098748 | |||||||
chr11:47098778 | A | T | 1 | a0001c0001t0001g0204 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.281-38867A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47098778 | |||||||
chr11:47099139 | C | A | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.281-38506C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099139 | |||||||
chr11:47099347 | C | A | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-38298C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099347 | |||||||
chr11:47099516 | C | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-38129C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099516 | |||||||
chr11:47099625 | T | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-38020T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099625 | |||||||
chr11:47099857 | G | A | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.281-37788G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099857 | |||||||
chr11:47099883 | A | C | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-37762A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099883 | |||||||
chr11:47099996 | C | G | 55 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-37649C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47099996 | |||||||
chr11:47100107 | T | C | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.281-37538T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100107 | |||||||
chr11:47100201 | A | T | 1 | a0001c0001t0002g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.281-37444A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100201 | |||||||
chr11:47100331 | T | A | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.281-37314T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100331 | |||||||
chr11:47100476 | A | C | 1 | a0001c0001t0001g0042 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.281-37169A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100476 | |||||||
chr11:47100541 | T | G | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-37104T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100541 | |||||||
chr11:47100871 | GC | G | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.281-36773delC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47100871 | |||||||
chr11:47101002 | A | AT | 27 | a0001c0001t0001g0001 a0001c0001t0001g0120 a0001c0001t0001g0191 others(24): Show |
27 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(24): Show |
intron_variant | MODIFIER | c.281-36628dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101002 | ||||||
chr11:47101164 | A | AT | 25 | a0001c0001t0001g0005 a0001c0001t0001g0011 a0001c0001t0001g0012 others(22): Show |
25 | HG00621.hp1 HG01109.hp2 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-36456dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATT | 9 | a0001c0001t0001g0077 a0001c0001t0001g0173 a0001c0001t0001g0195 others(6): Show |
9 | HG01109.hp1 HG01884.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-36457_281-3645 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTT | 9 | a0001c0001t0001g0179 a0001c0001t0001g0186 a0001c0001t0001g0191 others(6): Show |
9 | HG02109.hp1 HG02818.hp1 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-36458_281-3645 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTT | 8 | a0001c0001t0001g0143 a0001c0001t0001g0161 a0001c0001t0001g0197 others(5): Show |
8 | HG01261.hp1 HG02293.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-36459_281-3645 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTT | 20 | a0001c0001t0001g0076 a0001c0001t0001g0092 a0001c0001t0001g0104 others(17): Show |
20 | HG01257.hp2 HG01358.hp2 HG01993.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-36460_281-3645 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTT | 17 | a0001c0001t0001g0089 a0001c0001t0001g0095 a0001c0001t0001g0096 others(14): Show |
17 | HG00280.hp2 HG00597.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.281-36461_281-3645 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT | 8 | a0001c0001t0001g0082 a0001c0001t0001g0142 a0001c0001t0001g0146 others(5): Show |
8 | HG00733.hp2 HG02647.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-36462_281-3645 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(1): Show |
6 | a0001c0001t0001g0132 a0001c0001t0001g0136 a0001c0001t0001g0141 others(3): Show |
6 | HG01081.hp1 HG01496.hp1 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-36463_281-3645 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(2): Show |
16 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(13): Show |
16 | HG00438.hp1 HG00438.hp2 HG01192.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-36464_281-3645 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(3): Show |
4 | a0001c0001t0001g0139 a0001c0001t0001g0153 a0001c0001t0001g0157 others(1): Show |
4 | HG00673.hp1 HG01361.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-36465_281-3645 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(4): Show |
1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.281-36466_281-3645 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(5): Show |
2 | a0001c0001t0001g0154 a0001c0001t0001g0168 |
2 | HG00735.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.281-36467_281-3645 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(6): Show |
1 | a0001c0001t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.281-36468_281-3645 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(7): Show |
2 | a0001c0001t0001g0130 a0001c0001t0001g0189 |
2 | HG00738.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.281-36469_281-3645 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(9): Show |
1 | a0001c0001t0001g0187 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.281-36471_281-3645 others(20): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(10): Show |
1 | a0001c0001t0001g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.281-36472_281-3645 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101164 | A | ATTTTTTT others(16): Show |
1 | a0001c0001t0001g0175 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.281-36478_281-3645 others(27): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101164 | ||||||
chr11:47101185 | TTTTTATT others(3): Show |
T | 1 | a0004c0006t0001g0200 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.281-36455_281-3644 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47101185 | ||||||
chr11:47101188 | T | A | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.281-36457T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101188 | |||||||
chr11:47101189 | TA | T | 27 | a0001c0001t0001g0009 a0001c0001t0001g0013 a0001c0001t0001g0015 others(24): Show |
27 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.281-36455delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101189 | |||||||
chr11:47101190 | A | T | 187 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(184): Show |
187 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(184): Show |
intron_variant | MODIFIER | c.281-36455A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101190 | |||||||
chr11:47101195 | A | T | 141 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0076 others(138): Show |
141 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.281-36450A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101195 | |||||||
chr11:47101318 | T | A | 1 | a0001c0001t0001g0203 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.281-36327T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101318 | |||||||
chr11:47101402 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-36243G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101402 | |||||||
chr11:47101439 | T | C | 1 | a0001c0001t0001g0028 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.281-36206T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47101439 | |||||||
chr11:47102048 | G | A | 3 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0127 |
3 | NA18960.hp2 NA18978.hp2 NA19083.hp2 |
intron_variant | MODIFIER | c.281-35597G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102048 | |||||||
chr11:47102128 | T | C | 2 | a0003c0002t0001g0086 a0003c0002t0001g0087 |
2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.281-35517T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102128 | |||||||
chr11:47102183 | A | G | 4 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-35462A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102183 | |||||||
chr11:47102314 | A | C | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.281-35331A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102314 | |||||||
chr11:47102640 | T | A | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-35005T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102640 | |||||||
chr11:47102731 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0071 |
2 | NA18964.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.281-34914G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102731 | |||||||
chr11:47102774 | G | C | 1 | a0001c0001t0001g0117 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.281-34871G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47102774 | |||||||
chr11:47102989 | G | GA | 124 | a0001c0001t0001g0071 a0001c0001t0001g0076 a0001c0001t0001g0077 others(121): Show |
124 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(121): Show |
intron_variant | MODIFIER | c.281-34638dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47102989 | ||||||
chr11:47102989 | G | GAA | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(81): Show |
84 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.281-34639_281-3463 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47102989 | ||||||
chr11:47102989 | G | GAAA | 12 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0048 others(9): Show |
12 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.281-34640_281-3463 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47102989 | ||||||
chr11:47103110 | A | T | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-34535A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103110 | |||||||
chr11:47103399 | C | CA | 74 | a0001c0001t0001g0024 a0001c0001t0001g0070 a0001c0001t0001g0082 others(71): Show |
74 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(71): Show |
intron_variant | MODIFIER | c.281-34231dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47103399 | ||||||
chr11:47103590 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-34055T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103590 | |||||||
chr11:47103608 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281-34037C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103608 | |||||||
chr11:47103662 | A | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-33983A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103662 | |||||||
chr11:47103670 | C | CT | 5 | a0001c0001t0001g0050 a0001c0001t0001g0213 a0001c0001t0002g0207 others(2): Show |
5 | HG01109.hp2 HG02055.hp2 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-33951dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47103670 | ||||||
chr11:47103670 | CT | C | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(147): Show |
150 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(147): Show |
intron_variant | MODIFIER | c.281-33951delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47103670 | ||||||
chr11:47103778 | G | A | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-33867G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103778 | |||||||
chr11:47103806 | C | T | 16 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0106 others(13): Show |
16 | HG00609.hp1 HG00738.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.281-33839C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103806 | |||||||
chr11:47103838 | C | T | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-33807C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103838 | |||||||
chr11:47103851 | T | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-33794T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47103851 | |||||||
chr11:47104004 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-33641T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104004 | |||||||
chr11:47104081 | T | G | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.281-33564T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104081 | |||||||
chr11:47104096 | A | G | 1 | a0001c0001t0001g0155 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.281-33549A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104096 | |||||||
chr11:47104200 | G | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-33445G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104200 | |||||||
chr11:47104735 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.281-32910C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47104735 | |||||||
chr11:47105114 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.281-32531T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105114 | |||||||
chr11:47105391 | C | T | 1 | a0001c0001t0003g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.281-32254C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105391 | |||||||
chr11:47105602 | A | G | 7 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0129 others(4): Show |
7 | HG00438.hp1 HG02698.hp2 NA18947.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-32043A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105602 | |||||||
chr11:47105803 | T | G | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.281-31842T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105803 | |||||||
chr11:47105960 | T | C | 2 | a0001c0001t0001g0114 a0001c0001t0001g0118 |
2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.281-31685T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105960 | |||||||
chr11:47105998 | G | T | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-31647G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47105998 | |||||||
chr11:47106155 | G | A | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-31490G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106155 | |||||||
chr11:47106376 | A | G | 3 | a0001c0001t0001g0056 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG01071.hp2 HG03942.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.281-31269A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106376 | |||||||
chr11:47106488 | C | T | 2 | a0001c0001t0001g0025 a0001c0001t0001g0027 |
2 | HG02698.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.281-31157C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106488 | |||||||
chr11:47106642 | C | CA | 20 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(17): Show |
20 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-30991dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47106642 | ||||||
chr11:47106704 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.281-30941G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106704 | |||||||
chr11:47106737 | G | A | 14 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-30908G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47106737 | |||||||
chr11:47106795 | TAACCAAG others(6): Show |
T | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.281-30847_281-3083 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47106795 | ||||||
chr11:47107066 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.281-30579T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107066 | |||||||
chr11:47107177 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.281-30468G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107177 | |||||||
chr11:47107480 | T | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-30165T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107480 | |||||||
chr11:47107846 | C | T | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-29799C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107846 | |||||||
chr11:47107855 | T | TC | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-29783dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47107855 | ||||||
chr11:47107941 | C | G | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-29704C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47107941 | |||||||
chr11:47108303 | A | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-29342A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108303 | |||||||
chr11:47108415 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.281-29230C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108415 | |||||||
chr11:47108540 | C | A | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-29105C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108540 | |||||||
chr11:47108704 | C | CT | 183 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(180): Show |
183 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(180): Show |
intron_variant | MODIFIER | c.281-28921dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47108704 | ||||||
chr11:47108704 | C | CTT | 10 | a0001c0001t0001g0038 a0001c0001t0001g0044 a0001c0001t0001g0069 others(7): Show |
10 | HG00741.hp1 HG00741.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-28922_281-2892 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47108704 | ||||||
chr11:47108704 | CT | C | 20 | a0001c0001t0001g0048 a0001c0001t0001g0077 a0001c0001t0001g0078 others(17): Show |
20 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.281-28921delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47108704 | ||||||
chr11:47108732 | A | G | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.281-28913A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108732 | |||||||
chr11:47108761 | C | T | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.281-28884C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108761 | |||||||
chr11:47108810 | G | A | 4 | a0001c0001t0001g0139 a0001c0001t0001g0148 a0001c0001t0001g0149 others(1): Show |
4 | HG01934.hp1 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-28835G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108810 | |||||||
chr11:47108989 | G | C | 102 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(99): Show |
102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.281-28656G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47108989 | |||||||
chr11:47109082 | T | C | 4 | a0001c0001t0001g0108 a0001c0001t0001g0146 a0001c0001t0001g0147 others(1): Show |
4 | HG00733.hp2 HG00735.hp1 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-28563T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109082 | |||||||
chr11:47109227 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-28418G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109227 | |||||||
chr11:47109502 | C | G | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.281-28143C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109502 | |||||||
chr11:47109502 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-28143C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109502 | |||||||
chr11:47109779 | G | T | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-27866G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109779 | |||||||
chr11:47109957 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.281-27688T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47109957 | |||||||
chr11:47110160 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-27485C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110160 | |||||||
chr11:47110330 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-27315A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110330 | |||||||
chr11:47110470 | C | G | 2 | a0001c0001t0001g0112 a0001c0004t0001g0113 |
2 | HG01071.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.281-27175C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110470 | |||||||
chr11:47110581 | C | A | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-27064C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110581 | |||||||
chr11:47110628 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-27017C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110628 | |||||||
chr11:47110688 | T | C | 3 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0162 |
3 | HG03942.hp1 NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.281-26957T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110688 | |||||||
chr11:47110890 | C | CT | 6 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0164 others(3): Show |
6 | HG00738.hp2 HG01109.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-26738dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | ||||||
chr11:47110890 | C | CTTTTTTT | 32 | a0001c0001t0001g0004 a0001c0001t0001g0010 a0001c0001t0001g0020 others(29): Show |
32 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.281-26744_281-2673 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | ||||||
chr11:47110890 | C | CTTTTTTT others(1): Show |
54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(51): Show |
54 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.281-26745_281-2673 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | ||||||
chr11:47110890 | C | CTTTTTTT others(2): Show |
7 | a0001c0001t0001g0006 a0001c0001t0001g0016 a0001c0001t0001g0043 others(4): Show |
7 | HG01192.hp2 HG02080.hp1 NA18947.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-26746_281-2673 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | ||||||
chr11:47110890 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0056 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.281-26747_281-2673 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47110890 | ||||||
chr11:47110991 | G | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-26654G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47110991 | |||||||
chr11:47111173 | A | T | 76 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(73): Show |
76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.281-26472A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111173 | |||||||
chr11:47111209 | A | C | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-26436A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111209 | |||||||
chr11:47111531 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.281-26114C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111531 | |||||||
chr11:47111570 | C | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.281-26075C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111570 | |||||||
chr11:47111868 | C | G | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-25777C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47111868 | |||||||
chr11:47112053 | C | G | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-25592C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112053 | |||||||
chr11:47112131 | C | A | 2 | a0001c0001t0001g0116 a0001c0001t0001g0117 |
2 | NA18971.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.281-25514C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112131 | |||||||
chr11:47112313 | A | ATTTG | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-25312_281-2530 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47112313 | ||||||
chr11:47112348 | G | C | 1 | a0001c0001t0001g0138 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.281-25297G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112348 | |||||||
chr11:47112362 | C | G | 3 | a0001c0001t0001g0215 a0001c0001t0001g0216 a0001c0001t0001g0219 |
3 | HG03516.hp2 NA20129.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.281-25283C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47112362 | |||||||
chr11:47113357 | G | C | 1 | a0001c0001t0001g0078 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.281-24288G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47113357 | |||||||
chr11:47113806 | A | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-23839A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47113806 | |||||||
chr11:47113855 | G | A | 1 | a0001c0001t0001g0051 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.281-23790G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47113855 | |||||||
chr11:47114010 | G | C | 10 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0202 others(7): Show |
10 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-23635G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114010 | |||||||
chr11:47114131 | C | T | 3 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0164 |
3 | HG00738.hp2 HG01358.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.281-23514C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114131 | |||||||
chr11:47114328 | C | T | 14 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0037 others(11): Show |
14 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(11): Show |
intron_variant | MODIFIER | c.281-23317C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114328 | |||||||
chr11:47114424 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.281-23221C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114424 | |||||||
chr11:47114445 | A | G | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
216 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.281-23200A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114445 | |||||||
chr11:47114837 | G | T | 3 | a0001c0001t0001g0194 a0001c0001t0001g0197 a0001c0001t0001g0198 |
3 | HG02818.hp1 HG03225.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.281-22808G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47114837 | |||||||
chr11:47115272 | G | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-22373G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115272 | |||||||
chr11:47115512 | A | T | 2 | a0001c0001t0001g0192 a0004c0006t0001g0200 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.281-22133A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115512 | |||||||
chr11:47115521 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.281-22124C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115521 | |||||||
chr11:47115751 | A | T | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
216 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.281-21894A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115751 | |||||||
chr11:47115752 | A | T | 1 | a0001c0001t0001g0043 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.281-21893A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115752 | |||||||
chr11:47115956 | A | G | 5 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0106 others(2): Show |
5 | HG00738.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-21689A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47115956 | |||||||
chr11:47116113 | T | G | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.281-21532T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116113 | |||||||
chr11:47116303 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281-21342G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116303 | |||||||
chr11:47116427 | C | T | 1 | a0001c0001t0001g0141 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.281-21218C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116427 | |||||||
chr11:47116661 | C | T | 6 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0028 others(3): Show |
6 | HG00597.hp1 HG02132.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-20984C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116661 | |||||||
chr11:47116675 | G | GT | 143 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(140): Show |
143 | HG00280.hp1 HG00438.hp1 HG00597.hp2 others(140): Show |
intron_variant | MODIFIER | c.281-20948dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | ||||||
chr11:47116675 | G | GTT | 20 | a0001c0001t0001g0001 a0001c0001t0001g0029 a0001c0001t0001g0060 others(17): Show |
20 | HG00280.hp2 HG00597.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-20949_281-2094 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | ||||||
chr11:47116675 | GT | G | 25 | a0001c0001t0001g0072 a0001c0001t0001g0084 a0001c0001t0001g0090 others(22): Show |
25 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(22): Show |
intron_variant | MODIFIER | c.281-20948delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | ||||||
chr11:47116675 | GTTT | G | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-20950_281-2094 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47116675 | ||||||
chr11:47116805 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.281-20840G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47116805 | |||||||
chr11:47117142 | T | C | 1 | a0001c0001t0001g0066 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.281-20503T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117142 | |||||||
chr11:47117489 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-20156C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117489 | |||||||
chr11:47117512 | T | C | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-20133T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117512 | |||||||
chr11:47117703 | T | C | 5 | a0001c0001t0001g0091 a0001c0001t0001g0102 a0001c0001t0001g0106 others(2): Show |
5 | HG00738.hp2 HG01099.hp2 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-19942T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117703 | |||||||
chr11:47117862 | C | T | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-19783C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117862 | |||||||
chr11:47117877 | CT | C | 122 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(119): Show |
122 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(119): Show |
intron_variant | MODIFIER | c.281-19746delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47117877 | ||||||
chr11:47117877 | CTT | C | 83 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(80): Show |
83 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.281-19747_281-1974 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47117877 | ||||||
chr11:47117883 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-19762T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117883 | |||||||
chr11:47117914 | G | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-19731G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47117914 | |||||||
chr11:47118086 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.281-19559G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118086 | |||||||
chr11:47118209 | T | A | 1 | a0001c0001t0001g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.281-19436T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118209 | |||||||
chr11:47118401 | T | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.281-19244T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118401 | |||||||
chr11:47118508 | C | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-19137C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118508 | |||||||
chr11:47118526 | G | C | 1 | a0001c0001t0003g0159 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.281-19119G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118526 | |||||||
chr11:47118697 | T | A | 3 | a0001c0001t0001g0089 a0001c0001t0001g0119 a0001c0001t0001g0162 |
3 | HG03942.hp1 NA18983.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.281-18948T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118697 | |||||||
chr11:47118810 | T | G | 1 | a0001c0001t0001g0016 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.281-18835T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47118810 | |||||||
chr11:47119039 | T | A | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.281-18606T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119039 | |||||||
chr11:47119186 | G | C | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-18459G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119186 | |||||||
chr11:47119278 | A | T | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-18367A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119278 | |||||||
chr11:47119602 | CT | C | 50 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0010 others(47): Show |
50 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(47): Show |
intron_variant | MODIFIER | c.281-18017delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47119602 | ||||||
chr11:47119602 | CTT | C | 113 | a0001c0001t0001g0052 a0001c0001t0001g0074 a0001c0001t0001g0076 others(110): Show |
113 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(110): Show |
intron_variant | MODIFIER | c.281-18018_281-1801 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47119602 | ||||||
chr11:47119681 | G | A | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
65 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.281-17964G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119681 | |||||||
chr11:47119705 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-17940G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119705 | |||||||
chr11:47119749 | T | A | 1 | a0001c0001t0001g0017 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.281-17896T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119749 | |||||||
chr11:47119812 | C | T | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.281-17833C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119812 | |||||||
chr11:47119945 | C | T | 8 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(5): Show |
8 | HG00621.hp2 HG02080.hp2 HG03017.hp2 others(5): Show |
intron_variant | MODIFIER | c.281-17700C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47119945 | |||||||
chr11:47120119 | C | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-17526C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120119 | |||||||
chr11:47120515 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281-17130G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120515 | |||||||
chr11:47120634 | C | A | 4 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 others(1): Show |
4 | HG01243.hp1 HG01884.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-17011C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120634 | |||||||
chr11:47120695 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-16950C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120695 | |||||||
chr11:47120833 | A | G | 2 | a0001c0001t0001g0130 a0001c0001t0001g0151 |
2 | HG00738.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.281-16812A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47120833 | |||||||
chr11:47121111 | A | G | 1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.281-16534A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47121111 | |||||||
chr11:47121573 | T | G | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-16072T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47121573 | |||||||
chr11:47121796 | G | T | 1 | a0001c0001t0001g0013 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.281-15849G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47121796 | |||||||
chr11:47122069 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-15576C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122069 | |||||||
chr11:47122069 | C | CA | 6 | a0001c0001t0001g0076 a0001c0001t0001g0176 a0001c0001t0001g0177 others(3): Show |
6 | HG02451.hp2 HG02809.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-15553dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | C | CAAA | 5 | a0001c0001t0001g0091 a0001c0001t0001g0174 a0001c0001t0001g0180 others(2): Show |
5 | HG01099.hp2 HG02559.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15555_281-1555 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | C | CAAAA | 6 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0002g0196 others(3): Show |
6 | HG01071.hp1 HG01243.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.281-15556_281-1555 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | C | CAAAAA | 10 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0111 others(7): Show |
10 | HG00738.hp2 HG01109.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.281-15557_281-1555 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | C | CAAAAAAA others(3): Show |
1 | a0003c0002t0001g0087 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.281-15562_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | C | CAAAAAAA others(5): Show |
1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.281-15564_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | CAA | C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(5): Show |
8 | HG01081.hp2 HG01099.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-15554_281-1555 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | CAAAA | C | 41 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(38): Show |
41 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(38): Show |
intron_variant | MODIFIER | c.281-15556_281-1555 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122069 | CAAAAAAA | C | 5 | a0001c0001t0001g0049 a0001c0001t0001g0051 a0001c0001t0001g0052 others(2): Show |
5 | HG01515.hp2 HG02559.hp1 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15559_281-1555 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122069 | ||||||
chr11:47122087 | A | AATATATA others(3): Show |
1 | a0001c0001t0001g0125 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.281-15557_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122087 | ||||||
chr11:47122087 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0130 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.281-15558_281-1555 others(25): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122087 | |||||||
chr11:47122087 | A | T | 4 | a0001c0001t0001g0002 a0001c0001t0001g0046 a0001c0001t0001g0054 others(1): Show |
4 | HG01074.hp2 HG01261.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-15558A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122087 | |||||||
chr11:47122089 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0142 a0001c0001t0001g0154 |
2 | HG00735.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.281-15555_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | ||||||
chr11:47122089 | A | AATATATA others(5): Show |
2 | a0001c0001t0001g0160 a0002c0003t0001g0115 |
2 | HG00597.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.281-15555_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | ||||||
chr11:47122089 | A | AATATATA others(7): Show |
1 | a0001c0001t0001g0157 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.281-15555_281-1555 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | ||||||
chr11:47122089 | A | ATATATAT others(4): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0151 |
2 | HG03688.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.281-15556_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122089 | |||||||
chr11:47122089 | A | T | 11 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(8): Show |
11 | HG00621.hp2 HG00735.hp2 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.281-15556A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122089 | |||||||
chr11:47122089 | AAAAT | A | 5 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0056 others(2): Show |
5 | HG00280.hp1 HG00733.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-15554_281-1555 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122089 | ||||||
chr11:47122091 | A | AAAAAAAA others(8): Show |
1 | a0001c0001t0001g0072 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(19): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0041 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0003g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(28): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(6): Show |
3 | a0001c0001t0001g0099 a0001c0001t0003g0100 a0001c0001t0003g0159 |
3 | HG01081.hp1 HG01192.hp1 HG02602.hp2 |
intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(14): Show |
1 | a0001c0001t0001g0221 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(25): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(5): Show |
2 | a0001c0001t0001g0094 a0001c0001t0001g0168 |
2 | HG00642.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(15): Show |
1 | a0001c0001t0004g0220 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(26): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0223 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(28): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(6): Show |
4 | a0001c0001t0001g0084 a0001c0001t0001g0107 a0001c0001t0003g0097 others(1): Show |
4 | HG02004.hp2 HG03710.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0127 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(4): Show |
1 | a0003c0002t0001g0086 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0121 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(1): Show |
6 | a0001c0001t0001g0105 a0001c0001t0001g0116 a0001c0001t0001g0162 others(3): Show |
6 | HG02257.hp1 HG02257.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(3): Show |
1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAA others(5): Show |
1 | a0001c0001t0001g0146 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0158 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAAAT others(6): Show |
1 | a0001c0001t0001g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(17): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAATA others(5): Show |
1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(22): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAATAT | 5 | a0001c0001t0001g0126 a0001c0001t0001g0190 a0001c0001t0001g0191 others(2): Show |
5 | HG00673.hp1 HG03130.hp1 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAAATAT others(10): Show |
1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAATATA others(1): Show |
5 | a0001c0001t0001g0122 a0001c0001t0001g0124 a0001c0001t0001g0143 others(2): Show |
5 | HG02293.hp2 HG02300.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(12): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAATATA others(3): Show |
2 | a0001c0001t0001g0095 a0001c0001t0001g0155 |
2 | HG03831.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.281-15553_281-1555 others(14): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAAATATA others(5): Show |
1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.281-15553_281-1555 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAATATAT others(2): Show |
5 | a0001c0001t0001g0103 a0001c0001t0001g0104 a0001c0001t0001g0123 others(2): Show |
5 | HG02080.hp2 HG02698.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15553_281-1555 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AAATATAT others(4): Show |
1 | a0001c0001t0001g0133 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.281-15553_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | AATATATA others(5): Show |
2 | a0001c0001t0001g0108 a0001c0001t0001g0147 |
2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.281-15537_281-1552 others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47122091 | ||||||
chr11:47122091 | A | ATATAT | 2 | a0001c0001t0001g0148 a0001c0001t0001g0149 |
2 | HG01993.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.281-15554_281-1555 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | |||||||
chr11:47122091 | A | ATATATAT | 2 | a0001c0001t0001g0085 a0001c0001t0001g0165 |
2 | HG00438.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.281-15554_281-1555 others(11): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | |||||||
chr11:47122091 | A | ATATATAT others(2): Show |
5 | a0001c0001t0001g0082 a0001c0001t0001g0132 a0001c0001t0001g0141 others(2): Show |
5 | HG02809.hp2 NA18947.hp2 NA19011.hp1 others(2): Show |
intron_variant | MODIFIER | c.281-15554_281-1555 others(13): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | |||||||
chr11:47122091 | A | ATATATAT others(4): Show |
1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.281-15554_281-1555 others(15): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | |||||||
chr11:47122091 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.281-15554_281-1555 others(21): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | |||||||
chr11:47122091 | A | T | 39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0011 others(36): Show |
39 | HG00597.hp1 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.281-15554A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122091 | |||||||
chr11:47122093 | T | A | 19 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0109 others(16): Show |
19 | HG01099.hp2 HG01109.hp1 HG01884.hp2 others(16): Show |
intron_variant | MODIFIER | c.281-15552T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122093 | |||||||
chr11:47122095 | T | A | 8 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0176 others(5): Show |
8 | HG01109.hp1 HG02809.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.281-15550T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122095 | |||||||
chr11:47122097 | T | A | 1 | a0001c0001t0001g0179 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.281-15548T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122097 | |||||||
chr11:47122937 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-14708A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122937 | |||||||
chr11:47122991 | A | C | 65 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(62): Show |
65 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.281-14654A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47122991 | |||||||
chr11:47123385 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.281-14260A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123385 | |||||||
chr11:47123521 | G | A | 99 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(96): Show |
99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.281-14124G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123521 | |||||||
chr11:47123807 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281-13838C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123807 | |||||||
chr11:47123877 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281-13768G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47123877 | |||||||
chr11:47123939 | T | TGA | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-13705_281-1370 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47123939 | ||||||
chr11:47124064 | TATTGAGA others(21): Show |
T | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13579_281-1355 others(32): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124064 | ||||||
chr11:47124114 | C | CT | 99 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(96): Show |
99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.281-13504dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | ||||||
chr11:47124114 | C | CTT | 36 | a0001c0001t0001g0041 a0001c0001t0001g0084 a0001c0001t0001g0090 others(33): Show |
36 | HG00438.hp2 HG00642.hp1 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.281-13505_281-1350 others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | ||||||
chr11:47124114 | C | CTTT | 5 | a0001c0001t0001g0010 a0001c0001t0001g0072 a0001c0001t0001g0121 others(2): Show |
5 | HG01192.hp1 HG02145.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.281-13506_281-1350 others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | ||||||
chr11:47124114 | C | CTTTT | 6 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(3): Show |
6 | HG02622.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.281-13507_281-1350 others(8): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | ||||||
chr11:47124114 | C | CTTTTT | 42 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(39): Show |
42 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.281-13508_281-1350 others(9): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | ||||||
chr11:47124114 | C | CTTTTTT | 20 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0016 others(17): Show |
20 | HG00642.hp2 HG00735.hp2 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.281-13509_281-1350 others(10): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47124114 | ||||||
chr11:47124122 | T | TGGGTTTT others(25): Show |
1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13523_281-1352 others(36): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124122 | |||||||
chr11:47124126 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13519T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124126 | |||||||
chr11:47124130 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13515T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124130 | |||||||
chr11:47124134 | T | G | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13511T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124134 | |||||||
chr11:47124151 | G | T | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13494G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124151 | |||||||
chr11:47124160 | G | A | 1 | a0001c0001t0002g0217 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.281-13485G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124160 | |||||||
chr11:47124227 | A | C | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13418A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124227 | |||||||
chr11:47124312 | C | G | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13333C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124312 | |||||||
chr11:47124313 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.281-13332G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124313 | |||||||
chr11:47124523 | A | C | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.281-13122A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124523 | |||||||
chr11:47124629 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-13016C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124629 | |||||||
chr11:47124980 | CA | C | 2 | a0001c0001t0001g0038 a0001c0001t0001g0044 |
2 | NA18947.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.281-12664delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47124980 | |||||||
chr11:47125016 | C | G | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-12629C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125016 | |||||||
chr11:47125048 | C | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.281-12597C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125048 | |||||||
chr11:47125566 | C | A | 1 | a0001c0001t0001g0010 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.281-12079C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125566 | |||||||
chr11:47125838 | A | G | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-11807A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125838 | |||||||
chr11:47125874 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.281-11771G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125874 | |||||||
chr11:47125879 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.281-11766C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125879 | |||||||
chr11:47125955 | T | C | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.281-11690T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125955 | |||||||
chr11:47125970 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-11675T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47125970 | |||||||
chr11:47126659 | C | T | 99 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(96): Show |
99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.281-10986C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47126659 | |||||||
chr11:47126957 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.281-10688A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47126957 | |||||||
chr11:47127112 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-10533G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127112 | |||||||
chr11:47127177 | C | T | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-10468C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127177 | |||||||
chr11:47127848 | G | A | 2 | a0001c0001t0001g0202 a0001c0001t0001g0213 |
2 | HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.281-9797G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127848 | |||||||
chr11:47127879 | A | T | 206 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(203): Show |
206 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(203): Show |
intron_variant | MODIFIER | c.281-9766A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127879 | |||||||
chr11:47127882 | T | A | 1 | a0001c0001t0001g0073 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.281-9763T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127882 | |||||||
chr11:47127945 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.281-9700T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47127945 | |||||||
chr11:47128296 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.281-9349G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128296 | |||||||
chr11:47128434 | C | T | 7 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(4): Show |
7 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.281-9211C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128434 | |||||||
chr11:47128626 | G | A | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-9019G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128626 | |||||||
chr11:47128688 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.281-8957T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128688 | |||||||
chr11:47128696 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.281-8949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128696 | |||||||
chr11:47128882 | C | T | 3 | a0001c0001t0001g0078 a0001c0001t0001g0079 a0001c0001t0001g0080 |
3 | HG02723.hp2 HG03130.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.281-8763C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47128882 | |||||||
chr11:47129229 | C | T | 3 | a0001c0001t0001g0175 a0001c0001t0001g0184 a0001c0001t0001g0187 |
3 | HG01243.hp1 HG01884.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.281-8416C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129229 | |||||||
chr11:47129342 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.281-8303T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129342 | |||||||
chr11:47129420 | T | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.281-8225T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129420 | |||||||
chr11:47129576 | C | G | 1 | a0001c0001t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.281-8069C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47129576 | |||||||
chr11:47130030 | G | A | 1 | a0001c0001t0001g0024 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.281-7615G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130030 | |||||||
chr11:47130201 | G | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0212 |
2 | HG02257.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.281-7444G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130201 | |||||||
chr11:47130234 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.281-7411C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130234 | |||||||
chr11:47130255 | C | CA | 9 | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0080 others(6): Show |
9 | HG01934.hp2 HG02145.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.281-7377dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47130255 | ||||||
chr11:47130346 | G | A | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.281-7299G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130346 | |||||||
chr11:47130394 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.281-7251G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130394 | |||||||
chr11:47130635 | CCTT | C | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-7005_281-7003d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47130635 | ||||||
chr11:47130709 | C | T | 1 | a0001c0001t0001g0057 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.281-6936C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130709 | |||||||
chr11:47130722 | G | A | 76 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(73): Show |
76 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(73): Show |
intron_variant | MODIFIER | c.281-6923G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47130722 | |||||||
chr11:47131466 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-6179G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131466 | |||||||
chr11:47131702 | C | T | 4 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0042 others(1): Show |
4 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.281-5943C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131702 | |||||||
chr11:47131750 | G | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0126 |
2 | NA18949.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.281-5895G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131750 | |||||||
chr11:47131840 | A | G | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.281-5805A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131840 | |||||||
chr11:47131848 | A | G | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-5797A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131848 | |||||||
chr11:47131876 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.281-5769C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131876 | |||||||
chr11:47131963 | T | A | 3 | a0001c0001t0001g0201 a0001c0001t0001g0202 a0001c0001t0001g0213 |
3 | HG02109.hp1 HG02572.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.281-5682T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47131963 | |||||||
chr11:47132129 | G | A | 2 | a0001c0001t0001g0179 a0001c0001t0001g0186 |
2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.281-5516G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132129 | |||||||
chr11:47132181 | C | A | 1 | a0001c0001t0001g0124 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.281-5464C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132181 | |||||||
chr11:47132282 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.281-5363C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132282 | |||||||
chr11:47132472 | G | A | 1 | a0002c0003t0001g0115 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.281-5173G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132472 | |||||||
chr11:47132963 | A | G | 13 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(10): Show |
13 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.281-4682A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47132963 | |||||||
chr11:47133013 | A | G | 1 | a0001c0001t0001g0107 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.281-4632A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133013 | |||||||
chr11:47133143 | T | A | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.281-4502T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133143 | |||||||
chr11:47133408 | G | C | 1 | a0001c0001t0001g0111 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.281-4237G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133408 | |||||||
chr11:47133412 | G | C | 1 | a0001c0001t0001g0043 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.281-4233G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133412 | |||||||
chr11:47133672 | A | T | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-3973A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47133672 | |||||||
chr11:47134214 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.281-3431G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134214 | |||||||
chr11:47134214 | G | C | 18 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(15): Show |
18 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.281-3431G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134214 | |||||||
chr11:47134435 | T | C | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(214): Show |
217 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(214): Show |
intron_variant | MODIFIER | c.281-3210T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134435 | |||||||
chr11:47134510 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-3135C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134510 | |||||||
chr11:47134563 | C | T | 2 | a0001c0001t0001g0023 a0001c0001t0001g0171 |
2 | NA18983.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.281-3082C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134563 | |||||||
chr11:47134579 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.281-3066G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134579 | |||||||
chr11:47134876 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.281-2769C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134876 | |||||||
chr11:47134902 | A | G | 2 | a0001c0001t0001g0038 a0001c0001t0001g0044 |
2 | NA18947.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.281-2743A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47134902 | |||||||
chr11:47135154 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.281-2491G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47135154 | |||||||
chr11:47135266 | T | C | 1 | a0001c0001t0001g0090 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.281-2379T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47135266 | |||||||
chr11:47135679 | G | A | 7 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0120 others(4): Show |
7 | HG00621.hp2 HG02080.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.281-1966G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47135679 | |||||||
chr11:47135976 | A | ACT | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(63): Show |
66 | HG00280.hp1 HG00597.hp1 HG00642.hp2 others(63): Show |
intron_variant | MODIFIER | c.281-1649_281-1648d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr11 | 47135976 | ||||||
chr11:47136126 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-1519T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136126 | |||||||
chr11:47136284 | G | A | 1 | a0001c0001t0001g0194 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.281-1361G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136284 | |||||||
chr11:47136314 | C | T | 25 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0102 others(22): Show |
25 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.281-1331C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136314 | |||||||
chr11:47136315 | G | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(93): Show |
96 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(93): Show |
intron_variant | MODIFIER | c.281-1330G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136315 | |||||||
chr11:47136367 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.281-1278C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136367 | |||||||
chr11:47136369 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.281-1276G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136369 | |||||||
chr11:47136497 | A | C | 1 | a0001c0001t0001g0224 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.281-1148A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136497 | |||||||
chr11:47136841 | A | G | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.281-804A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47136841 | |||||||
chr11:47137071 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.281-574A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137071 | |||||||
chr11:47137168 | G | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.281-477G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137168 | |||||||
chr11:47137403 | C | T | 1 | a0001c0001t0001g0128 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.281-242C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137403 | |||||||
chr11:47137502 | G | A | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.281-143G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 3/8 | chr11 | 47137502 | |||||||
chr11:47137895 | T | C | 1 | a0001c0001t0001g0076 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.365+166T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47137895 | |||||||
chr11:47138013 | C | CCA | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+296_365+297dup others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138013 | ||||||
chr11:47138015 | A | C | 7 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(4): Show |
7 | HG02572.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+286A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138015 | |||||||
chr11:47138418 | G | A | 4 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0170 others(1): Show |
4 | HG01071.hp1 HG01515.hp1 HG02109.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+689G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138418 | |||||||
chr11:47138470 | G | A | 1 | a0001c0001t0001g0201 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.365+741G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138470 | |||||||
chr11:47138538 | G | A | 1 | a0001c0001t0001g0171 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.365+809G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138538 | |||||||
chr11:47138848 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.365+1119G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138848 | |||||||
chr11:47138895 | G | A | 1 | a0001c0001t0002g0209 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.365+1166G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47138895 | |||||||
chr11:47138979 | C | CA | 27 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0015 others(24): Show |
27 | HG00642.hp2 HG00735.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.365+1283dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | C | CAA | 18 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0011 others(15): Show |
18 | HG00280.hp1 HG00597.hp1 HG00733.hp1 others(15): Show |
intron_variant | MODIFIER | c.365+1282_365+1283d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | C | CAAA | 20 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(17): Show |
20 | HG00609.hp2 HG00621.hp1 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.365+1281_365+1283d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | C | CAAAA | 10 | a0001c0001t0001g0036 a0001c0001t0001g0041 a0001c0001t0001g0057 others(7): Show |
10 | HG00438.hp2 HG01081.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.365+1280_365+1283d others(6): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | C | CAAAAA | 8 | a0001c0001t0001g0043 a0001c0001t0001g0094 a0001c0001t0001g0107 others(5): Show |
8 | HG00642.hp1 HG01243.hp2 HG02004.hp2 others(5): Show |
intron_variant | MODIFIER | c.365+1279_365+1283d others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | CA | C | 39 | a0001c0001t0001g0010 a0001c0001t0001g0074 a0001c0001t0001g0076 others(36): Show |
39 | HG00280.hp2 HG00597.hp2 HG00621.hp2 others(36): Show |
intron_variant | MODIFIER | c.365+1283delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | CAA | C | 73 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0091 others(70): Show |
73 | HG00438.hp1 HG00609.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.365+1282_365+1283d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | CAAAAAAA others(9): Show |
C | 1 | a0001c0001t0001g0108 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.365+1268_365+1283d others(18): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47138979 | CAAAAAAA others(14): Show |
C | 1 | a0001c0001t0001g0116 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.365+1263_365+1283d others(23): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47138979 | ||||||
chr11:47139072 | C | T | 99 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(96): Show |
99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.365+1343C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139072 | |||||||
chr11:47139364 | C | T | 1 | a0001c0001t0001g0096 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.365+1635C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139364 | |||||||
chr11:47139421 | C | G | 1 | a0001c0001t0001g0123 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.365+1692C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139421 | |||||||
chr11:47139671 | C | CA | 6 | a0001c0001t0001g0010 a0001c0001t0001g0102 a0001c0001t0001g0221 others(3): Show |
6 | HG02055.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+1957dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47139671 | ||||||
chr11:47139671 | CA | C | 52 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(49): Show |
52 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.365+1957delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47139671 | ||||||
chr11:47139861 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.365+2132C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47139861 | |||||||
chr11:47140012 | T | C | 1 | a0001c0001t0001g0195 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.365+2283T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140012 | |||||||
chr11:47140096 | C | T | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+2367C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140096 | |||||||
chr11:47140970 | G | A | 1 | a0001c0001t0001g0011 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.365+3241G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140970 | |||||||
chr11:47140996 | G | C | 1 | a0001c0001t0002g0208 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.365+3267G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47140996 | |||||||
chr11:47141053 | T | G | 102 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(99): Show |
102 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(99): Show |
intron_variant | MODIFIER | c.365+3324T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141053 | |||||||
chr11:47141129 | T | A | 2 | a0001c0001t0001g0001 a0001c0001t0001g0066 |
2 | HG03017.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.365+3400T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141129 | |||||||
chr11:47141194 | A | T | 1 | a0001c0001t0001g0161 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.365+3465A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141194 | |||||||
chr11:47141367 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365+3638G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141367 | |||||||
chr11:47141766 | C | T | 1 | a0001c0001t0003g0093 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.365+4037C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141766 | |||||||
chr11:47141788 | C | T | 1 | a0001c0001t0001g0092 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.365+4059C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141788 | |||||||
chr11:47141932 | C | CA | 87 | a0001c0001t0001g0005 a0001c0001t0001g0024 a0001c0001t0001g0029 others(84): Show |
87 | HG00280.hp2 HG00597.hp1 HG00597.hp2 others(84): Show |
intron_variant | MODIFIER | c.365+4229dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | ||||||
chr11:47141932 | C | CAA | 35 | a0001c0001t0001g0036 a0001c0001t0001g0080 a0001c0001t0001g0085 others(32): Show |
35 | HG00438.hp1 HG00735.hp1 HG00741.hp2 others(32): Show |
intron_variant | MODIFIER | c.365+4228_365+4229d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | ||||||
chr11:47141932 | CA | C | 23 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0012 others(20): Show |
23 | HG00438.hp2 HG00642.hp1 HG00735.hp2 others(20): Show |
intron_variant | MODIFIER | c.365+4229delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | ||||||
chr11:47141932 | CAA | C | 10 | a0001c0001t0001g0072 a0001c0001t0001g0090 a0001c0001t0001g0099 others(7): Show |
10 | HG01081.hp1 HG01496.hp1 HG02004.hp2 others(7): Show |
intron_variant | MODIFIER | c.365+4228_365+4229d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | ||||||
chr11:47141932 | CAAAAA | C | 7 | a0001c0001t0001g0048 a0001c0001t0001g0049 a0001c0001t0001g0050 others(4): Show |
7 | HG02559.hp1 HG02622.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+4225_365+4229d others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47141932 | ||||||
chr11:47141971 | G | A | 1 | a0001c0001t0001g0145 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.365+4242G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47141971 | |||||||
chr11:47142191 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365+4462C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142191 | |||||||
chr11:47142241 | CA | C | 215 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(212): Show |
215 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(212): Show |
intron_variant | MODIFIER | c.365+4528delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47142241 | ||||||
chr11:47142261 | T | G | 2 | a0001c0001t0001g0221 a0001c0001t0004g0220 |
2 | HG02615.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.365+4532T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142261 | |||||||
chr11:47142573 | G | A | 1 | a0001c0001t0001g0162 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.365+4844G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142573 | |||||||
chr11:47142657 | G | C | 149 | a0001c0001t0001g0041 a0001c0001t0001g0048 a0001c0001t0001g0049 others(146): Show |
149 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.365+4928G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142657 | |||||||
chr11:47142888 | T | A | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.365+5159T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47142888 | |||||||
chr11:47143555 | G | A | 99 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(96): Show |
99 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.365+5826G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47143555 | |||||||
chr11:47143597 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.365+5868C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47143597 | |||||||
chr11:47143814 | A | G | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+6085A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47143814 | |||||||
chr11:47144270 | C | G | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+6541C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47144270 | |||||||
chr11:47144698 | G | C | 5 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0132 others(2): Show |
5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.365+6969G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47144698 | |||||||
chr11:47144800 | T | A | 7 | a0001c0001t0001g0191 a0001c0001t0001g0201 a0001c0001t0001g0202 others(4): Show |
7 | HG01261.hp1 HG02109.hp1 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.365+7071T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47144800 | |||||||
chr11:47144980 | A | AT | 20 | a0001c0001t0001g0091 a0001c0001t0001g0101 a0001c0001t0001g0102 others(17): Show |
20 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.365+7277dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | ||||||
chr11:47144980 | A | ATT | 49 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(46): Show |
49 | HG00280.hp2 HG00438.hp1 HG00673.hp1 others(46): Show |
intron_variant | MODIFIER | c.365+7276_365+7277d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | ||||||
chr11:47144980 | A | ATTT | 24 | a0001c0001t0001g0076 a0001c0001t0001g0096 a0001c0001t0001g0105 others(21): Show |
24 | HG00597.hp2 HG01243.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.365+7275_365+7277d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | ||||||
chr11:47144980 | ATT | A | 12 | a0001c0001t0001g0005 a0001c0001t0001g0009 a0001c0001t0001g0043 others(9): Show |
12 | HG00621.hp1 HG01978.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.365+7276_365+7277d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | ||||||
chr11:47144980 | ATTT | A | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(79): Show |
82 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.365+7275_365+7277d others(5): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | ||||||
chr11:47144980 | ATTTTTTT others(7): Show |
A | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+7264_365+7277d others(16): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47144980 | ||||||
chr11:47145135 | G | A | 1 | a0001c0001t0001g0061 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.365+7406G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47145135 | |||||||
chr11:47145328 | G | A | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.365+7599G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47145328 | |||||||
chr11:47145900 | A | ATTATT | 4 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0001g0190 others(1): Show |
4 | HG00673.hp1 HG02300.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+8200_365+8204d others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47145900 | ||||||
chr11:47145900 | A | ATTGTT | 25 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0195 others(22): Show |
25 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.365+8173_365+8174i others(7): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47145900 | ||||||
chr11:47146119 | T | C | 1 | a0001c0001t0001g0214 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.365+8390T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146119 | |||||||
chr11:47146152 | C | G | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.365+8423C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146152 | |||||||
chr11:47146238 | G | A | 73 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(70): Show |
73 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(70): Show |
intron_variant | MODIFIER | c.365+8509G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146238 | |||||||
chr11:47146365 | CA | C | 210 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(207): Show |
210 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(207): Show |
intron_variant | MODIFIER | c.365+8656delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47146365 | ||||||
chr11:47146658 | T | A | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366-8518T>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146658 | |||||||
chr11:47146703 | A | G | 10 | a0001c0001t0001g0001 a0001c0001t0001g0012 a0001c0001t0001g0046 others(7): Show |
10 | HG00735.hp2 HG01074.hp1 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.366-8473A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146703 | |||||||
chr11:47146752 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.366-8424G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146752 | |||||||
chr11:47146971 | G | A | 9 | a0001c0001t0001g0172 a0001c0001t0001g0176 a0001c0001t0001g0177 others(6): Show |
9 | HG02647.hp1 HG02809.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.366-8205G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47146971 | |||||||
chr11:47147632 | G | A | 1 | a0001c0001t0001g0029 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.366-7544G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47147632 | |||||||
chr11:47147677 | G | C | 55 | a0001c0001t0001g0002 a0001c0001t0001g0004 a0001c0001t0001g0005 others(52): Show |
55 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.366-7499G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47147677 | |||||||
chr11:47147825 | T | C | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.366-7351T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47147825 | |||||||
chr11:47148004 | G | A | 19 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(16): Show |
19 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.366-7172G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148004 | |||||||
chr11:47148422 | C | T | 1 | a0001c0001t0001g0054 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.366-6754C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148422 | |||||||
chr11:47148431 | T | C | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366-6745T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148431 | |||||||
chr11:47148896 | A | G | 1 | a0001c0001t0003g0098 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.366-6280A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47148896 | |||||||
chr11:47149231 | G | A | 1 | a0001c0001t0001g0018 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.366-5945G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47149231 | |||||||
chr11:47149465 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-5711T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47149465 | |||||||
chr11:47150163 | G | A | 6 | a0001c0001t0001g0094 a0001c0001t0003g0093 a0001c0001t0003g0097 others(3): Show |
6 | HG00642.hp1 HG01081.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-5013G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150163 | |||||||
chr11:47150200 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0126 |
2 | NA18949.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.366-4976C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150200 | |||||||
chr11:47150324 | T | C | 16 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.366-4852T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150324 | |||||||
chr11:47150520 | A | T | 1 | a0001c0001t0001g0080 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.366-4656A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150520 | |||||||
chr11:47150531 | C | A | 1 | a0001c0005t0001g0083 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.366-4645C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150531 | |||||||
chr11:47150571 | T | G | 1 | a0001c0007t0001g0063 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.366-4605T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47150571 | |||||||
chr11:47150883 | GT | G | 175 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(172): Show |
175 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(172): Show |
intron_variant | MODIFIER | c.366-4272delT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47150883 | ||||||
chr11:47151219 | C | T | 1 | a0001c0001t0001g0036 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.366-3957C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47151219 | |||||||
chr11:47151400 | C | CA | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
75 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.366-3764dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47151400 | ||||||
chr11:47151400 | CA | C | 16 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.366-3764delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47151400 | ||||||
chr11:47151505 | A | G | 12 | a0001c0001t0001g0192 a0001c0001t0002g0196 a0001c0001t0002g0199 others(9): Show |
12 | HG01109.hp2 HG01496.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.366-3671A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47151505 | |||||||
chr11:47151597 | C | CG | 216 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(213): Show |
216 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(213): Show |
intron_variant | MODIFIER | c.366-3573dupG | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47151597 | ||||||
chr11:47151722 | T | C | 4 | a0001c0001t0001g0077 a0001c0001t0001g0078 a0001c0001t0001g0079 others(1): Show |
4 | HG02572.hp2 HG02723.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.366-3454T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47151722 | |||||||
chr11:47152024 | C | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366-3152C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152024 | |||||||
chr11:47152242 | C | CA | 12 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0025 others(9): Show |
12 | HG00280.hp1 HG01071.hp2 HG02148.hp1 others(9): Show |
intron_variant | MODIFIER | c.366-2920dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47152242 | ||||||
chr11:47152242 | CA | C | 16 | a0001c0001t0001g0076 a0001c0001t0001g0172 a0001c0001t0001g0174 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.366-2920delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47152242 | ||||||
chr11:47152511 | G | A | 75 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(72): Show |
75 | HG00280.hp1 HG00597.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.366-2665G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152511 | |||||||
chr11:47152519 | G | A | 1 | a0001c0001t0001g0059 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.366-2657G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152519 | |||||||
chr11:47152533 | G | A | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2643G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152533 | |||||||
chr11:47152535 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2641G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152535 | |||||||
chr11:47152536 | G | C | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2640G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152536 | |||||||
chr11:47152539 | G | T | 1 | a0001c0001t0001g0110 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.366-2637G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152539 | |||||||
chr11:47152576 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.366-2600G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152576 | |||||||
chr11:47152745 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.366-2431C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152745 | |||||||
chr11:47152810 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.366-2366C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47152810 | |||||||
chr11:47153199 | TTA | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0132 others(2): Show |
5 | HG00438.hp1 NA18947.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.366-1975_366-1974d others(4): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47153199 | ||||||
chr11:47153227 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.366-1949T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153227 | |||||||
chr11:47153293 | G | T | 1 | a0001c0001t0001g0053 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.366-1883G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153293 | |||||||
chr11:47153584 | A | T | 1 | a0001c0001t0001g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.366-1592A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153584 | |||||||
chr11:47153599 | A | G | 48 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(45): Show |
48 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.366-1577A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153599 | |||||||
chr11:47153625 | G | A | 48 | a0001c0001t0001g0082 a0001c0001t0001g0085 a0001c0001t0001g0089 others(45): Show |
48 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(45): Show |
intron_variant | MODIFIER | c.366-1551G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153625 | |||||||
chr11:47153681 | C | T | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.366-1495C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153681 | |||||||
chr11:47153776 | G | A | 71 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0101 others(68): Show |
71 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.366-1400G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153776 | |||||||
chr11:47153896 | G | C | 1 | a0001c0001t0001g0001 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.366-1280G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153896 | |||||||
chr11:47153949 | G | T | 1 | a0001c0001t0001g0190 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.366-1227G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47153949 | |||||||
chr11:47154258 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.366-918A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154258 | |||||||
chr11:47154280 | G | A | 1 | a0001c0001t0001g0119 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.366-896G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154280 | |||||||
chr11:47154298 | T | C | 6 | a0001c0001t0001g0023 a0001c0001t0001g0026 a0001c0001t0001g0028 others(3): Show |
6 | HG00597.hp1 HG02132.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-878T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154298 | |||||||
chr11:47154454 | C | T | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.366-722C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154454 | |||||||
chr11:47154455 | G | A | 1 | a0001c0001t0001g0140 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.366-721G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47154455 | |||||||
chr11:47154867 | A | AC | 7 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0030 others(4): Show |
7 | HG01099.hp1 HG01261.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.366-304dupC | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr11 | 47154867 | ||||||
chr11:47155085 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.366-91C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 4/8 | chr11 | 47155085 | |||||||
chr11:47155453 | G | A | 1 | a0001c0001t0001g0027 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.451+192G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155453 | |||||||
chr11:47155880 | A | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(218): Show |
221 | HG00280.hp1 HG00280.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.451+619A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155880 | |||||||
chr11:47155956 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.451+695C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155956 | |||||||
chr11:47155957 | G | A | 1 | a0001c0001t0001g0068 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.451+696G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47155957 | |||||||
chr11:47156279 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.452-744T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156279 | |||||||
chr11:47156286 | C | T | 1 | a0001c0001t0001g0070 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.452-737C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156286 | |||||||
chr11:47156399 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.452-624A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156399 | |||||||
chr11:47156850 | A | C | 1 | a0001c0001t0001g0030 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.452-173A>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 5/8 | chr11 | 47156850 | |||||||
chr11:47157291 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0126 |
2 | NA18949.hp1 NA18991.hp1 |
intron_variant | MODIFIER | c.647+73C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157291 | |||||||
chr11:47157305 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.647+87C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157305 | |||||||
chr11:47157306 | G | T | 1 | a0001c0001t0001g0091 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.647+88G>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157306 | |||||||
chr11:47157434 | A | G | 26 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0193 others(23): Show |
26 | HG01109.hp2 HG01261.hp1 HG01496.hp2 others(23): Show |
intron_variant | MODIFIER | c.647+216A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157434 | |||||||
chr11:47157592 | C | T | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
169 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.648-221C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157592 | |||||||
chr11:47157610 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.648-203C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 6/8 | chr11 | 47157610 | |||||||
chr11:47158226 | G | C | 10 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0013 others(7): Show |
10 | HG00642.hp2 HG00733.hp1 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.757+304G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158226 | |||||||
chr11:47158278 | A | G | 121 | a0001c0001t0001g0076 a0001c0001t0001g0082 a0001c0001t0001g0085 others(118): Show |
121 | HG00280.hp2 HG00438.hp1 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.757+356A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158278 | |||||||
chr11:47158310 | C | A | 169 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(166): Show |
169 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.757+388C>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158310 | |||||||
chr11:47158343 | G | GA | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(94): Show |
97 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(94): Show |
intron_variant | MODIFIER | c.757+431dupA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47158343 | ||||||
chr11:47158621 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.757+699G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158621 | |||||||
chr11:47158836 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.757+914G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158836 | |||||||
chr11:47158893 | T | C | 5 | a0001c0001t0003g0093 a0001c0001t0003g0097 a0001c0001t0003g0098 others(2): Show |
5 | HG01081.hp1 HG01192.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.757+971T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47158893 | |||||||
chr11:47159417 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.757+1495T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159417 | |||||||
chr11:47159489 | G | A | 93 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(90): Show |
93 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(90): Show |
intron_variant | MODIFIER | c.757+1567G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159489 | |||||||
chr11:47159500 | A | T | 18 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(15): Show |
18 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.757+1578A>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159500 | |||||||
chr11:47159776 | C | T | 4 | a0001c0001t0001g0221 a0001c0001t0001g0223 a0001c0001t0001g0224 others(1): Show |
4 | HG02615.hp1 HG02922.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.758-1351C>T | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159776 | |||||||
chr11:47159914 | G | C | 1 | a0001c0001t0003g0097 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.758-1213G>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159914 | |||||||
chr11:47159936 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.758-1191G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47159936 | |||||||
chr11:47160299 | CA | C | 23 | a0001c0001t0001g0002 a0001c0001t0001g0009 a0001c0001t0001g0011 others(20): Show |
23 | HG00280.hp1 HG00642.hp2 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.758-807delA | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160299 | ||||||
chr11:47160299 | CAA | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(134): Show |
137 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.758-808_758-807del others(2): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160299 | ||||||
chr11:47160299 | CAAA | C | 9 | a0001c0001t0001g0031 a0001c0001t0001g0040 a0001c0001t0001g0048 others(6): Show |
9 | HG01081.hp1 HG01099.hp2 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.758-809_758-807del others(3): Show |
CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160299 | ||||||
chr11:47160556 | C | G | 1 | a0001c0001t0001g0077 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.758-571C>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160556 | |||||||
chr11:47160689 | A | AT | 20 | a0001c0001t0001g0041 a0001c0001t0001g0072 a0001c0001t0001g0084 others(17): Show |
20 | HG00438.hp2 HG00642.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.758-428dupT | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | INFO_REALIGN_3_PRIME | chr11 | 47160689 | ||||||
chr11:47160757 | T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.758-370T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160757 | |||||||
chr11:47160802 | A | G | 71 | a0001c0001t0001g0076 a0001c0001t0001g0091 a0001c0001t0001g0101 others(68): Show |
71 | HG00609.hp1 HG00621.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.758-325A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160802 | |||||||
chr11:47160817 | A | G | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.758-310A>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160817 | |||||||
chr11:47160819 | G | A | 98 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(95): Show |
98 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(95): Show |
intron_variant | MODIFIER | c.758-308G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47160819 | |||||||
chr11:47161014 | G | A | 1 | a0001c0001t0001g0031 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.758-113G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47161014 | |||||||
chr11:47161073 | T | C | 1 | a0001c0001t0001g0034 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.758-54T>C | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 7/8 | chr11 | 47161073 | |||||||
chr11:47161347 | T | G | 1 | a0001c0001t0001g0168 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.822-117T>G | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/8 | chr11 | 47161347 | |||||||
chr11:47161375 | G | A | 21 | a0001c0001t0001g0101 a0001c0001t0001g0103 a0001c0001t0001g0109 others(18): Show |
21 | HG00609.hp1 HG00621.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.822-89G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/8 | chr11 | 47161375 | |||||||
chr11:47161434 | G | A | 11 | a0001c0001t0001g0011 a0001c0001t0001g0037 a0001c0001t0001g0038 others(8): Show |
11 | HG01361.hp2 HG01975.hp1 HG01993.hp1 others(8): Show |
intron_variant | MODIFIER | c.822-30G>A | CSTPP1 | ENSG00000149179.14 | transcript | ENST00000278460.12 | protein_coding | 8/8 | chr11 | 47161434 |