Item | Value |
---|---|
geneid | 2589 |
ensemblid | ENSG00000141429.14 |
hgncid | 4123 |
symbol | GALNT1 |
name | polypeptide N-acetylgalactosaminyltransferase 1 |
refseq_nuc | NM_020474.4 |
refseq_prot | NP_065207.2 |
ensembl_nuc | ENST00000269195.6 |
ensembl_prot | ENSP00000269195.4 |
mane_status | MANE Select |
chr | chr18 |
start | 35581740 |
end | 35711834 |
strand | + |
ver | v1.2 |
region | chr18:35581740-35711834 |
region5000 | chr18:35576740-35716834 |
regionname0 | GALNT1_chr18_35581740_35711834 |
regionname5000 | GALNT1_chr18_35576740_35716834 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 559 | 305 | 94 | 62 | 107 | 12 | 28 | 80 | GALNT1_chr18_35576740_35716834 | GALNT1 | MRKFA others(554): Show |
chr18 | 35576740 | 35716834 |
a0002 | 0/0 | 559 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | MRKFA others(554): Show |
chr18 | 35576740 | 35716834 |
a0003 | 0/0 | 559 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | MRKFA others(554): Show |
chr18 | 35576740 | 35716834 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1677 | 298 | 87 | 62 | 107 | 12 | 28 | GALNT1_chr18_35576740_35716834 | GALNT1 | ATGAG others(1672): Show |
chr18 | 35576740 | 35716834 | ||
a0001c0003 | 0/0 | 1677 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | ATGAG others(1672): Show |
chr18 | 35576740 | 35716834 | ||
a0001c0004 | 0/0 | 1677 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | ATGAG others(1672): Show |
chr18 | 35576740 | 35716834 | ||
a0002c0002 | 0/0 | 1677 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | ATGAG others(1672): Show |
chr18 | 35576740 | 35716834 | ||
a0003c0005 | 0/0 | 1677 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | ATGAG others(1672): Show |
chr18 | 35576740 | 35716834 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3970 | 146 | 47 | 32 | 44 | 7 | 15 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0002 | 0/0 | 3970 | 42 | 12 | 7 | 17 | 2 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0003 | 0/0 | 3970 | 27 | 0 | 1 | 21 | 0 | 5 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0004 | 0/0 | 3970 | 27 | 4 | 14 | 6 | 3 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0005 | 0/0 | 3980 | 10 | 0 | 0 | 10 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3975): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0006 | 0/0 | 3971 | 7 | 3 | 4 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3966): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0007 | 0/0 | 3968 | 7 | 7 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3963): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0008 | 0/0 | 3974 | 6 | 0 | 0 | 6 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3969): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0009 | 0/0 | 3970 | 5 | 3 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0010 | 0/0 | 3966 | 4 | 0 | 0 | 0 | 0 | 4 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3961): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0011 | 0/0 | 3970 | 3 | 2 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0012 | 0/0 | 3970 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0013 | 0/0 | 3970 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0014 | 0/0 | 3970 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0015 | 0/0 | 3970 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0016 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0017 | 0/0 | 3970 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0018 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0019 | 0/0 | 3977 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3972): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0020 | 0/0 | 3976 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3971): Show |
chr18 | 35576740 | 35716834 |
a0001c0001t0021 | 0/1 | 3984 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3979): Show |
chr18 | 35576740 | 35716834 |
a0001c0003t0001 | 0/0 | 3970 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0001c0004t0001 | 0/0 | 3970 | 3 | 3 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0002c0002t0003 | 0/0 | 3970 | 4 | 0 | 0 | 4 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
a0003c0005t0001 | 0/0 | 3970 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | AGTGG others(3965): Show |
chr18 | 35576740 | 35716834 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0265 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0002 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0006g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0007g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0009g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0010g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0011g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0011g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0011g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0012g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0012g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0013g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0013g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0014g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0014g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0015g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0016g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0018g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0019g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0020g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0001t0021g0287 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0003t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0004t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0004t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0002c0002t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
a0003c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0102 | EUR | GBR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0017 | EUR | FIN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0196 | EUR | FIN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00408 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00558 | hp1 | a0001 | c0001 | t0008 | g0078 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00609 | hp1 | a0001 | c0001 | t0018 | g0033 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00621 | hp2 | a0001 | c0001 | t0004 | g0132 | EAS | CHS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0193 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01069 | hp1 | a0001 | c0001 | t0009 | g0155 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0151 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01074 | hp2 | a0001 | c0001 | t0004 | g0134 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01109 | hp1 | a0001 | c0001 | t0011 | g0254 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0144 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01243 | hp1 | a0001 | c0001 | t0002 | g0044 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01255 | hp2 | a0001 | c0001 | t0006 | g0156 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0149 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01261 | hp1 | a0001 | c0001 | t0015 | g0023 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01358 | hp1 | a0001 | c0001 | t0006 | g0157 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01433 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01496 | hp1 | a0001 | c0001 | t0004 | g0130 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0184 | AMR | CLM | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01515 | hp1 | a0001 | c0001 | t0004 | g0122 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0147 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01516 | hp1 | a0001 | c0001 | t0004 | g0123 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01884 | hp2 | a0001 | c0004 | t0001 | g0163 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01891 | hp1 | a0001 | c0001 | t0013 | g0164 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01928 | hp2 | a0001 | c0001 | t0004 | g0140 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01934 | hp1 | a0001 | c0001 | t0004 | g0142 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0001 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01975 | hp1 | a0001 | c0001 | t0004 | g0143 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01978 | hp2 | a0001 | c0001 | t0004 | g0150 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02015 | hp1 | a0003 | c0005 | t0001 | g0076 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02027 | hp1 | a0001 | c0001 | t0005 | g0064 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02055 | hp1 | a0001 | c0003 | t0001 | g0051 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0063 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02083 | hp1 | a0001 | c0001 | t0008 | g0080 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0258 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CDX | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02165 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | CDX | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02257 | hp1 | a0001 | c0001 | t0011 | g0260 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0125 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0145 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02280 | hp1 | a0001 | c0001 | t0007 | g0088 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02280 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0238 | AMR | PEL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02451 | hp1 | a0001 | c0001 | t0007 | g0104 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | KHV | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0280 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02615 | hp1 | a0001 | c0001 | t0009 | g0152 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02622 | hp1 | a0001 | c0001 | t0017 | g0047 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0173 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0027 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0188 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0262 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02818 | hp2 | a0001 | c0001 | t0009 | g0154 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02895 | hp1 | a0001 | c0001 | t0007 | g0089 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02895 | hp2 | a0001 | c0001 | t0012 | g0136 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0049 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02897 | hp2 | a0001 | c0001 | t0012 | g0138 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0264 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0158 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02965 | hp1 | a0001 | c0001 | t0007 | g0015 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02970 | hp2 | a0001 | c0003 | t0001 | g0050 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0248 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0011 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03041 | hp1 | a0001 | c0001 | t0012 | g0129 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03098 | hp1 | a0001 | c0001 | t0013 | g0162 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03139 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03195 | hp1 | a0001 | c0001 | t0014 | g0222 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03195 | hp2 | a0001 | c0004 | t0001 | g0126 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0048 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03486 | hp2 | a0001 | c0001 | t0007 | g0111 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03492 | hp1 | a0001 | c0001 | t0010 | g0011 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0261 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0161 | AFR | ESN | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03579 | hp2 | a0001 | c0001 | t0014 | g0221 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03669 | hp1 | a0001 | c0001 | t0010 | g0189 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0022 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0245 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0247 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0018 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0257 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0282 | SAS | STU | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18522 | hp1 | a0001 | c0001 | t0007 | g0112 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0006 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18747 | hp1 | a0001 | c0001 | t0005 | g0059 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | CHB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0006 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18948 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18951 | hp1 | a0001 | c0001 | t0005 | g0109 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18952 | hp2 | a0002 | c0002 | t0003 | g0243 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0251 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18960 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18960 | hp2 | a0001 | c0001 | t0008 | g0081 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0250 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18977 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18983 | hp1 | a0001 | c0001 | t0005 | g0062 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18988 | hp1 | a0001 | c0001 | t0008 | g0231 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18988 | hp2 | a0001 | c0001 | t0019 | g0056 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18990 | hp1 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18995 | hp1 | a0002 | c0002 | t0003 | g0242 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19001 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19005 | hp1 | a0001 | c0001 | t0005 | g0007 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0131 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19011 | hp2 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0263 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19055 | hp1 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0068 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19062 | hp1 | a0001 | c0001 | t0020 | g0052 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19062 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19064 | hp2 | a0002 | c0002 | t0003 | g0239 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19079 | hp1 | a0002 | c0002 | t0003 | g0241 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19084 | hp2 | a0001 | c0001 | t0008 | g0079 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | YRI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ASW | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0204 | AFR | ASW | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0028 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0095 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0253 | EUR | TSI | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02109 | hp1 | a0001 | c0001 | t0004 | g0124 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02109 | hp2 | a0001 | c0001 | t0016 | g0148 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02486 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0107 | AFR | ACB | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03471 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG03471 | hp2 | a0001 | c0001 | t0006 | g0159 | AFR | MSL | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0269 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0215 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | USA | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0256 | AFR | LWK | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
homoSapiens | chm13v2 | a0001 | c0001 | t0021 | g0287 | REF | REF | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0265 | REF | REF | GALNT1_chr18_35576740_35716834 | GALNT1 | chr18 | 35576740 | 35716834 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35654720 | T | G | 1 | a0002 | 4 | NA18952.hp2 NA18995.hp1 NA19064.hp2 others(1): Show |
missense_variant | MODERATE | c.58T>G | p.Leu20Val | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/12 | 284/3970 | 58/1680 | 20/559 | chr18 | 35654720 | |||
chr18:35709712 | A | G | 1 | a0003 | 1 | HG02015.hp1 | missense_variant | MODERATE | c.1622A>G | p.Asn541Ser | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1848/3970 | 1622/1680 | 541/559 | chr18 | 35709712 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35677684 | C | T | 1 | a0001c0003 | 4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
synonymous_variant | LOW | c.408C>T | p.Val136Val | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/12 | 634/3970 | 408/1680 | 136/559 | chr18 | 35677684 | |||
chr18:35703550 | C | T | 1 | a0001c0004 | 3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
synonymous_variant | LOW | c.1440C>T | p.Asp480Asp | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/12 | 1666/3970 | 1440/1680 | 480/559 | chr18 | 35703550 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35581786 | T | C | 1 | a0001c0001t0015 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-180T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72877 | chr18 | 35581786 | ||||||
chr18:35581833 | T | TGCTGCC | 3 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 |
12 | HG02027.hp1 HG02074.hp1 NA18747.hp1 others(9): Show |
5_prime_UTR_variant | MODIFIER | c.-131_-130insTGCCGC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/12 | 72827 | INFO_REALIGN_3_PRIME | chr18 | 35581833 | |||||
chr18:35654568 | C | T | 2 | a0001c0001t0004 a0001c0001t0012 |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/12 | chr18 | 35654568 | |||||||
chr18:35709902 | A | G | 1 | a0001c0001t0011 | 3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*132A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 132 | chr18 | 35709902 | ||||||
chr18:35710096 | C | G | 1 | a0001c0001t0014 | 2 | HG03195.hp1 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*326C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 326 | chr18 | 35710096 | ||||||
chr18:35710136 | C | T | 1 | a0001c0001t0009 | 5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*366C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 366 | chr18 | 35710136 | ||||||
chr18:35710150 | G | A | 1 | a0001c0001t0012 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*380G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 380 | chr18 | 35710150 | ||||||
chr18:35710473 | G | GA | 2 | a0001c0001t0006 a0001c0001t0019 |
8 | HG00642.hp1 HG01255.hp2 HG01358.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*712dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 713 | INFO_REALIGN_3_PRIME | chr18 | 35710473 | |||||
chr18:35710506 | TTC | T | 1 | a0001c0001t0007 | 7 | HG02280.hp1 HG02451.hp1 HG02559.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*743delCT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 742 | INFO_REALIGN_3_PRIME | chr18 | 35710506 | |||||
chr18:35710506 | TTCTC | T | 1 | a0001c0001t0010 | 4 | HG02735.hp2 HG03017.hp2 HG03492.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*740_*743delCTCT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 740 | INFO_REALIGN_3_PRIME | chr18 | 35710506 | |||||
chr18:35710655 | T | C | 1 | a0001c0001t0016 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*885T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 885 | chr18 | 35710655 | ||||||
chr18:35710714 | C | CTGAT | 2 | a0001c0001t0005 a0001c0001t0008 |
16 | HG00558.hp1 HG02027.hp1 HG02074.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*946_*949dupGATT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 950 | INFO_REALIGN_3_PRIME | chr18 | 35710714 | |||||
chr18:35710795 | A | T | 1 | a0001c0001t0018 | 1 | HG00609.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1025A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1025 | chr18 | 35710795 | ||||||
chr18:35711230 | G | C | 1 | a0001c0001t0017 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1460G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1460 | chr18 | 35711230 | ||||||
chr18:35711359 | C | T | 1 | a0001c0001t0013 | 2 | HG01891.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1589C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1589 | chr18 | 35711359 | ||||||
chr18:35711429 | A | G | 4 | a0001c0001t0003 a0001c0001t0019 a0001c0001t0020 others(1): Show |
33 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1659A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1659 | chr18 | 35711429 | ||||||
chr18:35711438 | A | G | 4 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0017 others(1): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1668A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 12/12 | 1668 | chr18 | 35711438 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr18:35581883 | T | C | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-104+21T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35581883 | |||||||
chr18:35582055 | T | C | 113 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(110): Show |
121 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.-104+193T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582055 | |||||||
chr18:35582064 | G | C | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-104+202G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582064 | |||||||
chr18:35582306 | A | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-104+444A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582306 | |||||||
chr18:35582446 | G | C | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+584G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582446 | |||||||
chr18:35582519 | C | A | 1 | a0001c0001t0007g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-104+657C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582519 | |||||||
chr18:35582651 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+789G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582651 | |||||||
chr18:35582796 | G | A | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+934G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582796 | |||||||
chr18:35582816 | T | C | 1 | a0001c0001t0001g0010 | 2 | HG00140.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.-104+954T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582816 | |||||||
chr18:35582896 | T | A | 13 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(10): Show |
13 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104+1034T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582896 | |||||||
chr18:35582915 | T | A | 1 | a0001c0001t0002g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-104+1053T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582915 | |||||||
chr18:35582929 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-104+1067C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582929 | |||||||
chr18:35582961 | T | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+1099T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35582961 | |||||||
chr18:35583243 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+1381A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583243 | |||||||
chr18:35583265 | A | G | 1 | a0001c0001t0001g0286 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-104+1403A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583265 | |||||||
chr18:35583328 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+1466A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583328 | |||||||
chr18:35583385 | T | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+1523T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583385 | |||||||
chr18:35583395 | C | T | 18 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+1533C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583395 | |||||||
chr18:35583458 | T | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-104+1596T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583458 | |||||||
chr18:35583518 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+1656C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583518 | |||||||
chr18:35583519 | A | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+1657A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583519 | |||||||
chr18:35583695 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+1833A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583695 | |||||||
chr18:35583958 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+2096A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35583958 | |||||||
chr18:35584070 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+2208A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584070 | |||||||
chr18:35584211 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+2349A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584211 | |||||||
chr18:35584290 | T | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-104+2428T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584290 | |||||||
chr18:35584428 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+2566A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584428 | |||||||
chr18:35584438 | A | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+2576A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584438 | |||||||
chr18:35584573 | A | G | 2 | a0001c0001t0001g0283 a0001c0001t0001g0284 |
2 | HG01891.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-104+2711A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584573 | |||||||
chr18:35584637 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-104+2775A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584637 | |||||||
chr18:35584689 | C | G | 2 | a0001c0001t0004g0149 a0001c0001t0004g0150 |
2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-104+2827C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584689 | |||||||
chr18:35584718 | T | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+2856T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584718 | |||||||
chr18:35584803 | A | G | 1 | a0001c0001t0003g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-104+2941A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584803 | |||||||
chr18:35584998 | A | G | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-104+3136A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35584998 | |||||||
chr18:35585119 | C | G | 46 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(43): Show |
52 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-104+3257C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35585119 | |||||||
chr18:35585721 | T | C | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG00639.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-104+3859T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35585721 | |||||||
chr18:35585885 | G | A | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-104+4023G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35585885 | |||||||
chr18:35586006 | T | G | 53 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0170 others(50): Show |
56 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-104+4144T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586006 | |||||||
chr18:35586092 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-104+4230G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586092 | |||||||
chr18:35586112 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-104+4250C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586112 | |||||||
chr18:35586233 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+4371C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586233 | |||||||
chr18:35586259 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104+4397A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586259 | |||||||
chr18:35586561 | GT | G | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-104+4704delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35586561 | ||||||
chr18:35586613 | G | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+4751G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586613 | |||||||
chr18:35586719 | A | T | 1 | a0001c0004t0001g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-104+4857A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586719 | |||||||
chr18:35586770 | T | G | 1 | a0001c0001t0001g0116 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-104+4908T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586770 | |||||||
chr18:35586788 | T | C | 1 | a0001c0001t0003g0220 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-104+4926T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35586788 | |||||||
chr18:35587019 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+5157G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587019 | |||||||
chr18:35587125 | C | CG | 9 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0003t0001g0048 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+5265dupG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35587125 | ||||||
chr18:35587229 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+5367A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587229 | |||||||
chr18:35587280 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+5418A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587280 | |||||||
chr18:35587300 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-104+5438G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587300 | |||||||
chr18:35587399 | G | A | 9 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0003t0001g0048 others(6): Show |
9 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+5537G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587399 | |||||||
chr18:35587420 | G | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+5558G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587420 | |||||||
chr18:35587505 | G | A | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+5643G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587505 | |||||||
chr18:35587576 | G | GT | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-104+5720dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35587576 | ||||||
chr18:35587756 | T | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+5894T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35587756 | |||||||
chr18:35588133 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+6271G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588133 | |||||||
chr18:35588312 | A | C | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-104+6450A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588312 | |||||||
chr18:35588335 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+6473C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588335 | |||||||
chr18:35588369 | C | T | 5 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0125 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+6507C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588369 | |||||||
chr18:35588370 | G | A | 1 | a0001c0001t0003g0004 | 3 | NA18939.hp1 NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.-104+6508G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588370 | |||||||
chr18:35588379 | T | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+6517T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588379 | |||||||
chr18:35588397 | G | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+6535G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588397 | |||||||
chr18:35588408 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-104+6546G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35588408 | |||||||
chr18:35588790 | GTTTA | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+6935_-104+693 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35588790 | ||||||
chr18:35589011 | G | A | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-104+7149G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589011 | |||||||
chr18:35589080 | G | A | 1 | a0001c0001t0003g0223 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-104+7218G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589080 | |||||||
chr18:35589170 | A | G | 58 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(55): Show |
65 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.-104+7308A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589170 | |||||||
chr18:35589215 | G | A | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+7353G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589215 | |||||||
chr18:35589327 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-104+7465T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589327 | |||||||
chr18:35589491 | T | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+7629T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589491 | |||||||
chr18:35589820 | T | G | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-104+7958T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35589820 | |||||||
chr18:35590362 | A | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+8500A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590362 | |||||||
chr18:35590390 | C | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | NA18965.hp2 NA19007.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-104+8528C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590390 | |||||||
chr18:35590410 | T | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+8548T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590410 | |||||||
chr18:35590458 | G | A | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-104+8596G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590458 | |||||||
chr18:35590467 | G | A | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-104+8605G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590467 | |||||||
chr18:35590702 | ACT | A | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+8844_-104+884 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35590702 | ||||||
chr18:35590785 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+8923A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35590785 | |||||||
chr18:35591012 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+9150C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591012 | |||||||
chr18:35591097 | G | A | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-104+9235G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591097 | |||||||
chr18:35591188 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-104+9326A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591188 | |||||||
chr18:35591848 | A | G | 7 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0003t0001g0048 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-104+9986A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35591848 | |||||||
chr18:35592011 | G | A | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01192.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-104+10149G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592011 | |||||||
chr18:35592170 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+10308C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592170 | |||||||
chr18:35592553 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-104+10691A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592553 | |||||||
chr18:35592857 | G | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+10995G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592857 | |||||||
chr18:35592865 | T | C | 36 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(33): Show |
40 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-104+11003T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35592865 | |||||||
chr18:35593135 | A | G | 52 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(49): Show |
58 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(55): Show |
intron_variant | MODIFIER | c.-104+11273A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593135 | |||||||
chr18:35593184 | G | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-104+11322G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593184 | |||||||
chr18:35593191 | C | T | 1 | a0001c0001t0004g0147 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-104+11329C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593191 | |||||||
chr18:35593419 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-104+11557A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593419 | |||||||
chr18:35593487 | C | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+11625C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593487 | |||||||
chr18:35593555 | GA | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+11694delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593555 | |||||||
chr18:35593557 | C | T | 7 | a0001c0001t0002g0002 a0001c0001t0002g0161 a0001c0001t0002g0165 others(4): Show |
11 | HG02257.hp2 HG02258.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.-104+11695C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593557 | |||||||
chr18:35593681 | T | G | 2 | a0001c0003t0001g0048 a0001c0003t0001g0049 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-104+11819T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593681 | |||||||
chr18:35593771 | C | T | 1 | a0001c0001t0001g0113 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-104+11909C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593771 | |||||||
chr18:35593924 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+12062G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35593924 | |||||||
chr18:35594057 | G | A | 284 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(281): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-104+12195G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594057 | |||||||
chr18:35594095 | C | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+12233C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594095 | |||||||
chr18:35594384 | C | T | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-104+12522C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594384 | |||||||
chr18:35594488 | G | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-104+12626G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594488 | |||||||
chr18:35594619 | A | G | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-104+12757A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594619 | |||||||
chr18:35594911 | T | C | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+13049T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594911 | |||||||
chr18:35594927 | C | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+13065C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35594927 | |||||||
chr18:35595009 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-104+13147A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595009 | |||||||
chr18:35595025 | A | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+13163A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595025 | |||||||
chr18:35595091 | G | A | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+13229G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595091 | |||||||
chr18:35595425 | A | T | 1 | a0001c0001t0017g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104+13563A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595425 | |||||||
chr18:35595527 | T | G | 1 | a0001c0001t0002g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-104+13665T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595527 | |||||||
chr18:35595599 | A | G | 1 | a0001c0001t0002g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-104+13737A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595599 | |||||||
chr18:35595674 | A | AT | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+13820dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35595674 | ||||||
chr18:35595700 | CA | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+13840delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35595700 | ||||||
chr18:35595702 | A | G | 81 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(78): Show |
91 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.-104+13840A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595702 | |||||||
chr18:35595703 | T | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+13841T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35595703 | |||||||
chr18:35596007 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-104+14145G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596007 | |||||||
chr18:35596039 | C | T | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+14177C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596039 | |||||||
chr18:35596082 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+14220A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596082 | |||||||
chr18:35596195 | T | A | 1 | a0001c0001t0002g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-104+14333T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596195 | |||||||
chr18:35596273 | G | C | 1 | a0001c0001t0001g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-104+14411G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596273 | |||||||
chr18:35596313 | A | T | 2 | a0001c0001t0004g0149 a0001c0001t0004g0150 |
2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-104+14451A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596313 | |||||||
chr18:35596314 | T | C | 2 | a0001c0001t0004g0149 a0001c0001t0004g0150 |
2 | HG01257.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.-104+14452T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596314 | |||||||
chr18:35596651 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-104+14789C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596651 | |||||||
chr18:35596674 | A | G | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.-104+14812A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596674 | |||||||
chr18:35596923 | T | C | 1 | a0001c0001t0001g0225 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-104+15061T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596923 | |||||||
chr18:35596950 | T | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+15088T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35596950 | |||||||
chr18:35597002 | C | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+15140C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597002 | |||||||
chr18:35597265 | A | G | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-104+15403A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597265 | |||||||
chr18:35597381 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+15519G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597381 | |||||||
chr18:35597519 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+15657A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597519 | |||||||
chr18:35597529 | G | A | 98 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(95): Show |
109 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.-104+15667G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597529 | |||||||
chr18:35597678 | C | T | 14 | a0001c0001t0002g0002 a0001c0001t0002g0161 a0001c0001t0002g0165 others(11): Show |
18 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+15816C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597678 | |||||||
chr18:35597679 | G | T | 11 | a0001c0001t0002g0002 a0001c0001t0002g0161 a0001c0001t0002g0165 others(8): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+15817G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597679 | |||||||
chr18:35597695 | A | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-104+15833A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597695 | |||||||
chr18:35597744 | A | C | 3 | a0001c0001t0005g0108 a0001c0001t0005g0109 a0001c0001t0005g0110 |
3 | NA18948.hp1 NA18951.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.-104+15882A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597744 | |||||||
chr18:35597863 | A | AAATGCTG others(365): Show |
1 | a0001c0001t0001g0170 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.-104+16017_-104+16 others(378): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597863 | ||||||
chr18:35597916 | T | A | 11 | a0001c0001t0002g0002 a0001c0001t0002g0161 a0001c0001t0002g0165 others(8): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+16054T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597916 | |||||||
chr18:35597931 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-104+16069A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597931 | |||||||
chr18:35597955 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+16093T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35597955 | |||||||
chr18:35597988 | A | ACTCCC | 28 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0210 others(25): Show |
30 | HG00408.hp1 HG00609.hp1 HG01175.hp2 others(27): Show |
intron_variant | MODIFIER | c.-104+16156_-104+16 others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | ||||||
chr18:35597988 | A | ACTCCCCT others(3): Show |
11 | a0001c0001t0001g0127 a0001c0001t0002g0016 a0001c0001t0002g0017 others(8): Show |
11 | HG00280.hp1 HG01168.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.-104+16151_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | ||||||
chr18:35597988 | A | ACTCCCCT others(8): Show |
3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01074.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-104+16146_-104+16 others(21): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | ||||||
chr18:35597988 | A | ACTCCCCT others(18): Show |
2 | a0001c0001t0001g0211 a0001c0001t0004g0124 |
2 | HG02109.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-104+16136_-104+16 others(31): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35597988 | ||||||
chr18:35598013 | CCTCCCCT others(3): Show |
C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+16152_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598013 | |||||||
chr18:35598014 | C | CTCCCCTC others(3): Show |
8 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0229 others(5): Show |
9 | HG01891.hp1 HG02257.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.-104+16160_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598014 | ||||||
chr18:35598014 | CTCCCCTC others(3): Show |
C | 6 | a0001c0001t0001g0057 a0001c0001t0001g0065 a0001c0001t0004g0139 others(3): Show |
6 | HG01358.hp2 HG02109.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+16161_-104+16 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598014 | ||||||
chr18:35598014 | CTCCCCTC others(13): Show |
C | 17 | a0001c0001t0004g0001 a0001c0001t0004g0128 a0001c0001t0004g0130 others(14): Show |
21 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-104+16161_-104+16 others(26): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598014 | ||||||
chr18:35598019 | CTCCAA | C | 25 | a0001c0001t0001g0058 a0001c0001t0001g0060 a0001c0001t0001g0061 others(22): Show |
26 | HG01069.hp1 HG01071.hp1 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.-104+16161_-104+16 others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598019 | ||||||
chr18:35598023 | A | C | 232 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(229): Show |
250 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(247): Show |
intron_variant | MODIFIER | c.-104+16161A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598023 | |||||||
chr18:35598024 | A | C | 54 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(51): Show |
56 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(53): Show |
intron_variant | MODIFIER | c.-104+16162A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598024 | |||||||
chr18:35598088 | G | T | 11 | a0001c0001t0002g0002 a0001c0001t0002g0161 a0001c0001t0002g0165 others(8): Show |
15 | HG02055.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+16226G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598088 | |||||||
chr18:35598104 | G | A | 3 | a0001c0001t0001g0069 a0001c0001t0014g0221 a0001c0001t0014g0222 |
3 | HG02735.hp1 HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+16242G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598104 | |||||||
chr18:35598148 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-104+16286G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598148 | |||||||
chr18:35598388 | C | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+16526C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598388 | |||||||
chr18:35598574 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+16712G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598574 | |||||||
chr18:35598576 | C | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+16714C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598576 | |||||||
chr18:35598713 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+16851A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598713 | |||||||
chr18:35598875 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104+17013C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35598875 | |||||||
chr18:35598991 | G | GT | 13 | a0001c0001t0001g0208 a0001c0001t0001g0216 a0001c0001t0001g0284 others(10): Show |
13 | HG00280.hp1 HG01069.hp1 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.-104+17146dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598991 | ||||||
chr18:35598991 | GT | G | 23 | a0001c0001t0001g0116 a0001c0001t0001g0119 a0001c0001t0001g0120 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.-104+17146delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598991 | ||||||
chr18:35598991 | GTT | G | 8 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 others(5): Show |
15 | HG01255.hp2 HG01358.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.-104+17145_-104+17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35598991 | ||||||
chr18:35599033 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+17171G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599033 | |||||||
chr18:35599283 | A | G | 2 | a0001c0003t0001g0048 a0001c0003t0001g0049 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-104+17421A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599283 | |||||||
chr18:35599366 | C | CCTTTT | 10 | a0001c0001t0002g0002 a0001c0001t0002g0018 a0001c0001t0002g0027 others(7): Show |
14 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-104+17504_-104+17 others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599366 | |||||||
chr18:35599366 | C | CCTTTTT | 23 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(20): Show |
25 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.-104+17504_-104+17 others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599366 | |||||||
chr18:35599366 | C | CCTTTTTT | 12 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(9): Show |
12 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-104+17504_-104+17 others(13): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599366 | |||||||
chr18:35599366 | C | CT | 84 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(81): Show |
90 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(87): Show |
intron_variant | MODIFIER | c.-104+17524dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35599366 | ||||||
chr18:35599366 | C | CTT | 18 | a0001c0001t0001g0014 a0001c0001t0001g0103 a0001c0001t0001g0168 others(15): Show |
19 | HG00609.hp2 HG00639.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-104+17523_-104+17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35599366 | ||||||
chr18:35599366 | C | CTTT | 24 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(21): Show |
28 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.-104+17522_-104+17 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35599366 | ||||||
chr18:35599387 | A | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+17525A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599387 | |||||||
chr18:35599816 | T | G | 49 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(46): Show |
55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-104+17954T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35599816 | |||||||
chr18:35600015 | T | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+18153T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600015 | |||||||
chr18:35600051 | G | T | 28 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(25): Show |
32 | HG01069.hp1 HG01071.hp1 HG01074.hp2 others(29): Show |
intron_variant | MODIFIER | c.-104+18189G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600051 | |||||||
chr18:35600095 | T | G | 1 | a0001c0001t0017g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104+18233T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600095 | |||||||
chr18:35600332 | G | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+18470G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600332 | |||||||
chr18:35600451 | A | G | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+18589A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600451 | |||||||
chr18:35600492 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-104+18630C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600492 | |||||||
chr18:35600495 | A | G | 4 | a0001c0001t0001g0202 a0001c0001t0001g0203 a0001c0001t0001g0204 others(1): Show |
4 | HG00639.hp1 HG01175.hp1 HG01243.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+18633A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600495 | |||||||
chr18:35600641 | A | G | 1 | a0001c0001t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-104+18779A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600641 | |||||||
chr18:35600668 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0113 others(1): Show |
5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+18806G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600668 | |||||||
chr18:35600674 | A | T | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+18812A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600674 | |||||||
chr18:35600676 | T | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+18814T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600676 | |||||||
chr18:35600746 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-104+18884C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600746 | |||||||
chr18:35600782 | G | A | 1 | a0001c0001t0001g0053 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-104+18920G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600782 | |||||||
chr18:35600869 | C | T | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+19007C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35600869 | |||||||
chr18:35600989 | CT | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+19133delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35600989 | ||||||
chr18:35601255 | A | G | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-104+19393A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601255 | |||||||
chr18:35601292 | T | C | 49 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(46): Show |
55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.-104+19430T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601292 | |||||||
chr18:35601400 | T | C | 1 | a0001c0001t0001g0074 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-104+19538T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601400 | |||||||
chr18:35601517 | G | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+19655G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601517 | |||||||
chr18:35601600 | C | T | 1 | a0001c0001t0004g0145 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-104+19738C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601600 | |||||||
chr18:35601615 | T | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+19753T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601615 | |||||||
chr18:35601664 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-104+19802T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601664 | |||||||
chr18:35601705 | C | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+19843C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601705 | |||||||
chr18:35601744 | G | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+19882G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601744 | |||||||
chr18:35601877 | T | G | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-104+20015T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601877 | |||||||
chr18:35601884 | G | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | NA18946.hp1 NA18986.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-104+20022G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35601884 | |||||||
chr18:35602040 | A | G | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104+20178A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602040 | |||||||
chr18:35602056 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+20194G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602056 | |||||||
chr18:35602153 | AT | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(23): Show |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-104+20299delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35602153 | ||||||
chr18:35602211 | T | C | 1 | a0001c0001t0003g0232 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-104+20349T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602211 | |||||||
chr18:35602344 | G | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+20482G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602344 | |||||||
chr18:35602457 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+20595C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602457 | |||||||
chr18:35602472 | C | T | 1 | a0001c0001t0003g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-104+20610C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602472 | |||||||
chr18:35602544 | C | T | 1 | a0001c0001t0017g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-104+20682C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602544 | |||||||
chr18:35602545 | A | G | 280 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(277): Show |
303 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(300): Show |
intron_variant | MODIFIER | c.-104+20683A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602545 | |||||||
chr18:35602625 | TCTCCTGT others(5): Show |
T | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+20765_-104+20 others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35602625 | ||||||
chr18:35602724 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+20862G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602724 | |||||||
chr18:35602794 | T | C | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+20932T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602794 | |||||||
chr18:35602864 | A | G | 125 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(122): Show |
137 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.-104+21002A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602864 | |||||||
chr18:35602923 | T | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+21061T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35602923 | |||||||
chr18:35603021 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-104+21159G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603021 | |||||||
chr18:35603059 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+21197G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603059 | |||||||
chr18:35603069 | G | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+21207G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603069 | |||||||
chr18:35603121 | T | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+21259T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603121 | |||||||
chr18:35603176 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+21314G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603176 | |||||||
chr18:35603228 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-104+21366C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603228 | |||||||
chr18:35603301 | G | T | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-104+21439G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603301 | |||||||
chr18:35603309 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+21447G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603309 | |||||||
chr18:35603453 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+21591G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603453 | |||||||
chr18:35603737 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+21875A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603737 | |||||||
chr18:35603822 | G | A | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+21960G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603822 | |||||||
chr18:35603823 | C | A | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+21961C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603823 | |||||||
chr18:35603869 | A | G | 1 | a0001c0001t0001g0073 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.-104+22007A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603869 | |||||||
chr18:35603922 | A | AT | 5 | a0001c0001t0001g0255 a0001c0001t0003g0235 a0001c0001t0011g0254 others(2): Show |
5 | HG01109.hp1 HG02257.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+22067dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35603922 | ||||||
chr18:35603993 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(189): Show |
210 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.-104+22131C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35603993 | |||||||
chr18:35604004 | T | G | 1 | a0001c0001t0003g0236 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.-104+22142T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604004 | |||||||
chr18:35604083 | T | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+22221T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604083 | |||||||
chr18:35604119 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0229 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+22257C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604119 | |||||||
chr18:35604268 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+22406C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604268 | |||||||
chr18:35604269 | G | A | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+22407G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604269 | |||||||
chr18:35604357 | A | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+22495A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604357 | |||||||
chr18:35604414 | T | C | 3 | a0001c0001t0006g0158 a0001c0001t0006g0159 a0001c0001t0006g0160 |
3 | HG02647.hp1 HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-104+22552T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35604414 | |||||||
chr18:35604427 | A | AATAC | 7 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
10 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.-104+22570_-104+22 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35604427 | ||||||
chr18:35604965 | T | TA | 3 | a0001c0001t0003g0235 a0001c0001t0014g0221 a0001c0001t0014g0222 |
3 | HG03195.hp1 HG03579.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-104+23108dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35604965 | ||||||
chr18:35605073 | A | G | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104+23211A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605073 | |||||||
chr18:35605265 | T | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+23403T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605265 | |||||||
chr18:35605282 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+23420G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605282 | |||||||
chr18:35605295 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+23433C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605295 | |||||||
chr18:35605325 | C | T | 2 | a0001c0001t0002g0018 a0001c0001t0002g0027 |
2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-104+23463C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605325 | |||||||
chr18:35605490 | CA | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+23642delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35605490 | ||||||
chr18:35605505 | G | A | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+23643G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605505 | |||||||
chr18:35605516 | A | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0113 others(1): Show |
5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+23654A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605516 | |||||||
chr18:35605555 | A | T | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+23693A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605555 | |||||||
chr18:35605597 | C | CT | 4 | a0001c0001t0001g0168 a0001c0001t0003g0235 a0001c0001t0013g0162 others(1): Show |
4 | HG00639.hp2 HG01884.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-104+23742dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35605597 | ||||||
chr18:35605872 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+24010G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605872 | |||||||
chr18:35605933 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+24071G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35605933 | |||||||
chr18:35606050 | C | T | 69 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(66): Show |
72 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(69): Show |
intron_variant | MODIFIER | c.-104+24188C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606050 | |||||||
chr18:35606069 | T | G | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+24207T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606069 | |||||||
chr18:35606167 | G | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+24305G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606167 | |||||||
chr18:35606170 | G | A | 2 | a0001c0001t0001g0229 a0001c0001t0001g0230 |
2 | HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-104+24308G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606170 | |||||||
chr18:35606190 | T | C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0229 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+24328T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606190 | |||||||
chr18:35606203 | A | C | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+24341A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606203 | |||||||
chr18:35606270 | C | T | 1 | a0001c0001t0003g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-104+24408C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606270 | |||||||
chr18:35606394 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+24532T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606394 | |||||||
chr18:35606557 | A | G | 1 | a0001c0001t0003g0200 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-104+24695A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606557 | |||||||
chr18:35606702 | C | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+24840C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606702 | |||||||
chr18:35606754 | C | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+24892C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606754 | |||||||
chr18:35606821 | T | TTG | 35 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0168 others(32): Show |
36 | HG00280.hp2 HG00558.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-104+25009_-104+25 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | T | TTGTG | 23 | a0001c0001t0001g0010 a0001c0001t0001g0176 a0001c0001t0001g0177 others(20): Show |
24 | HG00140.hp1 HG00609.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-104+25007_-104+25 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | T | TTGTGTGT others(3): Show |
1 | a0001c0001t0011g0256 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-104+25001_-104+25 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTG | T | 35 | a0001c0001t0001g0014 a0001c0001t0001g0170 a0001c0001t0001g0179 others(32): Show |
40 | HG00280.hp1 HG00621.hp1 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.-104+25009_-104+25 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTG | T | 31 | a0001c0001t0001g0014 a0001c0001t0001g0185 a0001c0001t0001g0187 others(28): Show |
31 | HG00639.hp1 HG01074.hp1 HG01175.hp1 others(28): Show |
intron_variant | MODIFIER | c.-104+25007_-104+25 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTGTG | T | 14 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0001g0066 others(11): Show |
14 | HG00408.hp2 HG01243.hp1 HG01516.hp2 others(11): Show |
intron_variant | MODIFIER | c.-104+25005_-104+25 others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTGTGT others(1): Show |
T | 61 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(58): Show |
67 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(64): Show |
intron_variant | MODIFIER | c.-104+25003_-104+25 others(14): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTGTGT others(3): Show |
T | 5 | a0001c0001t0001g0065 a0001c0001t0003g0250 a0001c0001t0007g0088 others(2): Show |
5 | HG01358.hp2 HG02280.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.-104+25001_-104+25 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTGTGT others(5): Show |
T | 2 | a0001c0001t0001g0086 a0001c0001t0013g0164 |
2 | HG01891.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-104+24999_-104+25 others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTGTGT others(9): Show |
T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-104+24995_-104+25 others(22): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606821 | TTGTGTGT others(19): Show |
T | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+24985_-104+25 others(32): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35606821 | ||||||
chr18:35606827 | G | C | 1 | a0001c0001t0003g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-104+24965G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606827 | |||||||
chr18:35606830 | T | A | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-104+24968T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606830 | |||||||
chr18:35606838 | T | A | 27 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0058 others(24): Show |
29 | HG00558.hp1 HG01069.hp2 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.-104+24976T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35606838 | |||||||
chr18:35607018 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+25156C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607018 | |||||||
chr18:35607026 | A | G | 1 | a0001c0001t0001g0105 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-104+25164A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607026 | |||||||
chr18:35607246 | A | G | 3 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0001g0102 |
3 | HG00140.hp2 HG00642.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.-104+25384A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607246 | |||||||
chr18:35607342 | G | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+25480G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607342 | |||||||
chr18:35607376 | A | G | 193 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(190): Show |
211 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(208): Show |
intron_variant | MODIFIER | c.-104+25514A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607376 | |||||||
chr18:35607507 | G | GCC | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-104+25646_-104+25 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35607507 | ||||||
chr18:35607589 | GC | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+25728delC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607589 | |||||||
chr18:35607660 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+25798C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607660 | |||||||
chr18:35607711 | G | C | 123 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(120): Show |
135 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-104+25849G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607711 | |||||||
chr18:35607712 | T | G | 161 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(158): Show |
177 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.-104+25850T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607712 | |||||||
chr18:35607728 | A | G | 123 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(120): Show |
135 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-104+25866A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607728 | |||||||
chr18:35607770 | T | A | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+25908T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607770 | |||||||
chr18:35607779 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-104+25917A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35607779 | |||||||
chr18:35608155 | G | T | 1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+26293G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608155 | |||||||
chr18:35608163 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+26301A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608163 | |||||||
chr18:35608164 | T | A | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+26302T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608164 | |||||||
chr18:35608206 | G | A | 28 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0220 others(25): Show |
30 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(27): Show |
intron_variant | MODIFIER | c.-104+26344G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608206 | |||||||
chr18:35608364 | C | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+26502C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608364 | |||||||
chr18:35608429 | C | G | 1 | a0001c0001t0002g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-104+26567C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608429 | |||||||
chr18:35608454 | G | GCCTTGGT others(15): Show |
1 | a0001c0001t0003g0235 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-104+26606_-104+26 others(28): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35608454 | ||||||
chr18:35608519 | G | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-104+26657G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608519 | |||||||
chr18:35608570 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+26708C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608570 | |||||||
chr18:35608606 | T | C | 76 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(73): Show |
82 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.-104+26744T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608606 | |||||||
chr18:35608691 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+26829C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608691 | |||||||
chr18:35608813 | C | T | 18 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-104+26951C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608813 | |||||||
chr18:35608881 | A | G | 121 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(118): Show |
133 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-104+27019A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608881 | |||||||
chr18:35608882 | T | C | 80 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(77): Show |
86 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(83): Show |
intron_variant | MODIFIER | c.-104+27020T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35608882 | |||||||
chr18:35609317 | ATC | A | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+27459_-104+27 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35609317 | ||||||
chr18:35609770 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+27908C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35609770 | |||||||
chr18:35610008 | T | G | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-104+28146T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610008 | |||||||
chr18:35610135 | A | G | 1 | a0001c0001t0003g0258 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-104+28273A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610135 | |||||||
chr18:35610167 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-104+28305T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610167 | |||||||
chr18:35610188 | G | A | 1 | a0001c0001t0004g0134 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-104+28326G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610188 | |||||||
chr18:35610588 | G | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+28726G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610588 | |||||||
chr18:35610658 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+28796G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610658 | |||||||
chr18:35610680 | A | C | 1 | a0001c0001t0002g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-104+28818A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610680 | |||||||
chr18:35610814 | G | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+28952G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610814 | |||||||
chr18:35610857 | G | C | 1 | a0001c0001t0001g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-104+28995G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610857 | |||||||
chr18:35610970 | G | C | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-104+29108G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35610970 | |||||||
chr18:35611015 | AGACCCCT others(15): Show |
A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+29164_-104+29 others(28): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35611015 | ||||||
chr18:35611079 | T | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+29217T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611079 | |||||||
chr18:35611113 | A | T | 1 | a0001c0001t0001g0230 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-104+29251A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611113 | |||||||
chr18:35611175 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+29313G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611175 | |||||||
chr18:35611185 | G | A | 1 | a0001c0001t0001g0180 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-104+29323G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611185 | |||||||
chr18:35611263 | A | C | 160 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(157): Show |
176 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.-104+29401A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611263 | |||||||
chr18:35611355 | T | A | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-104+29493T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611355 | |||||||
chr18:35611368 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+29506A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611368 | |||||||
chr18:35611545 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-104+29683A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611545 | |||||||
chr18:35611588 | T | C | 124 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
136 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-104+29726T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611588 | |||||||
chr18:35611738 | G | T | 36 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(33): Show |
40 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(37): Show |
intron_variant | MODIFIER | c.-104+29876G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611738 | |||||||
chr18:35611811 | C | T | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG00639.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-104+29949C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611811 | |||||||
chr18:35611848 | T | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+29986T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611848 | |||||||
chr18:35611950 | C | A | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+30088C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35611950 | |||||||
chr18:35612199 | G | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+30337G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612199 | |||||||
chr18:35612280 | C | T | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+30418C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612280 | |||||||
chr18:35612453 | C | T | 1 | a0001c0001t0007g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-104+30591C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612453 | |||||||
chr18:35612636 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-104+30774C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612636 | |||||||
chr18:35612865 | CAA | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-104+31015_-104+31 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35612865 | ||||||
chr18:35612882 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+31020G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612882 | |||||||
chr18:35612980 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+31118T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35612980 | |||||||
chr18:35613026 | G | A | 1 | a0001c0001t0004g0135 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-104+31164G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613026 | |||||||
chr18:35613124 | C | G | 79 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(76): Show |
85 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(82): Show |
intron_variant | MODIFIER | c.-104+31262C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613124 | |||||||
chr18:35613206 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-104+31344C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613206 | |||||||
chr18:35613248 | C | T | 119 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(116): Show |
131 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-104+31386C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613248 | |||||||
chr18:35613347 | G | GGCA | 28 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0058 others(25): Show |
30 | HG00558.hp1 HG01069.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.-104+31487_-104+31 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35613347 | ||||||
chr18:35613359 | G | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+31497G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613359 | |||||||
chr18:35613365 | A | G | 1 | a0001c0001t0002g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-104+31503A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613365 | |||||||
chr18:35613376 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+31514A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613376 | |||||||
chr18:35613423 | T | A | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-104+31561T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613423 | |||||||
chr18:35613434 | G | A | 1 | a0003c0005t0001g0076 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-104+31572G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613434 | |||||||
chr18:35613510 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-104+31648A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613510 | |||||||
chr18:35613828 | A | ACT | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+31969_-104+31 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35613828 | ||||||
chr18:35613875 | G | GA | 85 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(82): Show |
95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-104+32013_-104+32 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613875 | |||||||
chr18:35613876 | G | A | 87 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-104+32014G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35613876 | |||||||
chr18:35614085 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-104+32223G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614085 | |||||||
chr18:35614156 | T | G | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-104+32294T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614156 | |||||||
chr18:35614572 | A | G | 63 | a0001c0001t0001g0127 a0001c0001t0001g0225 a0001c0001t0001g0279 others(60): Show |
71 | HG00280.hp1 HG00621.hp2 HG01074.hp1 others(68): Show |
intron_variant | MODIFIER | c.-104+32710A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614572 | |||||||
chr18:35614705 | G | A | 39 | a0001c0001t0001g0226 a0001c0001t0002g0002 a0001c0001t0002g0005 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.-104+32843G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614705 | |||||||
chr18:35614730 | T | A | 6 | a0001c0001t0001g0127 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.-104+32868T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614730 | |||||||
chr18:35614921 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+33059A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614921 | |||||||
chr18:35614922 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+33060G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614922 | |||||||
chr18:35614942 | G | A | 55 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(52): Show |
62 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.-104+33080G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35614942 | |||||||
chr18:35615005 | C | T | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-104+33143C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615005 | |||||||
chr18:35615007 | A | G | 3 | a0001c0001t0001g0226 a0001c0004t0001g0125 a0001c0004t0001g0126 |
3 | HG02258.hp2 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-104+33145A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615007 | |||||||
chr18:35615210 | T | C | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-104+33348T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615210 | |||||||
chr18:35615289 | C | T | 1 | a0001c0001t0001g0283 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-104+33427C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615289 | |||||||
chr18:35615323 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-104+33461A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615323 | |||||||
chr18:35615392 | G | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+33530G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615392 | |||||||
chr18:35615398 | A | AC | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-104+33537dupC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35615398 | ||||||
chr18:35615422 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-104+33560A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615422 | |||||||
chr18:35615522 | G | A | 74 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
80 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.-104+33660G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615522 | |||||||
chr18:35615938 | G | A | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-104+34076G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615938 | |||||||
chr18:35615969 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+34107C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35615969 | |||||||
chr18:35616001 | A | G | 1 | a0001c0001t0001g0178 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.-104+34139A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616001 | |||||||
chr18:35616074 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-104+34212A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616074 | |||||||
chr18:35616218 | G | C | 1 | a0001c0001t0003g0257 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-104+34356G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616218 | |||||||
chr18:35616382 | T | G | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-104+34520T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616382 | |||||||
chr18:35616565 | G | A | 1 | a0002c0002t0003g0239 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104+34703G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616565 | |||||||
chr18:35616566 | C | G | 1 | a0002c0002t0003g0239 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104+34704C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616566 | |||||||
chr18:35616647 | G | A | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-104+34785G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616647 | |||||||
chr18:35616665 | C | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-104+34803C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616665 | |||||||
chr18:35616675 | G | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-104+34813G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616675 | |||||||
chr18:35616717 | G | A | 1 | a0001c0001t0002g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-104+34855G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616717 | |||||||
chr18:35616720 | A | G | 40 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(37): Show |
42 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.-104+34858A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616720 | |||||||
chr18:35616820 | C | A | 2 | a0001c0001t0001g0058 a0001c0001t0001g0077 |
2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-104+34958C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616820 | |||||||
chr18:35616888 | G | C | 1 | a0002c0002t0003g0239 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-104+35026G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616888 | |||||||
chr18:35616938 | T | A | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+35076T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35616938 | |||||||
chr18:35617060 | G | A | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-104+35198G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617060 | |||||||
chr18:35617082 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-104+35220G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617082 | |||||||
chr18:35617236 | G | C | 5 | a0001c0001t0001g0182 a0001c0001t0001g0183 a0001c0001t0001g0207 others(2): Show |
5 | NA18942.hp2 NA18990.hp2 NA19001.hp1 others(2): Show |
intron_variant | MODIFIER | c.-104+35374G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617236 | |||||||
chr18:35617301 | C | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-104+35439C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617301 | |||||||
chr18:35617412 | C | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0083 |
2 | HG01928.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.-104+35550C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617412 | |||||||
chr18:35617413 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-104+35551G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617413 | |||||||
chr18:35617424 | T | C | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+35562T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617424 | |||||||
chr18:35617440 | G | T | 1 | a0003c0005t0001g0076 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-104+35578G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617440 | |||||||
chr18:35617812 | T | G | 45 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-104+35950T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35617812 | |||||||
chr18:35618035 | C | CT | 31 | a0001c0001t0001g0102 a0001c0001t0001g0217 a0001c0001t0002g0022 others(28): Show |
35 | HG00140.hp2 HG00621.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.-104+36188dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35618035 | ||||||
chr18:35618035 | CT | C | 6 | a0001c0001t0001g0070 a0001c0001t0001g0174 a0001c0001t0013g0162 others(3): Show |
6 | HG00558.hp2 HG01167.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-104+36188delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35618035 | ||||||
chr18:35618169 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-104+36307C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618169 | |||||||
chr18:35618273 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-36287A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618273 | |||||||
chr18:35618313 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-103-36247T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618313 | |||||||
chr18:35618473 | G | A | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-36087G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618473 | |||||||
chr18:35618770 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-35790T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35618770 | |||||||
chr18:35619001 | A | G | 1 | a0001c0001t0001g0278 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-103-35559A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619001 | |||||||
chr18:35619097 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.-103-35463T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619097 | |||||||
chr18:35619230 | T | C | 1 | a0001c0001t0002g0043 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-103-35330T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619230 | |||||||
chr18:35619286 | T | G | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-35274T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619286 | |||||||
chr18:35619419 | A | G | 1 | a0001c0001t0001g0014 | 2 | HG02559.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-103-35141A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619419 | |||||||
chr18:35619621 | C | G | 6 | a0001c0001t0003g0004 a0001c0001t0003g0220 a0001c0001t0003g0223 others(3): Show |
8 | HG00408.hp2 HG02523.hp2 NA18612.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103-34939C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619621 | |||||||
chr18:35619705 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-34855C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619705 | |||||||
chr18:35619707 | C | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-34853C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619707 | |||||||
chr18:35619711 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-34849G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619711 | |||||||
chr18:35619718 | C | T | 1 | a0001c0001t0001g0099 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-103-34842C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619718 | |||||||
chr18:35619789 | G | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-34771G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619789 | |||||||
chr18:35619952 | T | C | 45 | a0001c0001t0001g0127 a0001c0001t0004g0001 a0001c0001t0004g0122 others(42): Show |
49 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(46): Show |
intron_variant | MODIFIER | c.-103-34608T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619952 | |||||||
chr18:35619975 | A | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-34585A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35619975 | |||||||
chr18:35620056 | A | G | 1 | a0001c0001t0007g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-103-34504A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620056 | |||||||
chr18:35620075 | G | A | 1 | a0001c0001t0007g0104 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-103-34485G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620075 | |||||||
chr18:35620112 | T | C | 1 | a0001c0001t0005g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-103-34448T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620112 | |||||||
chr18:35620125 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-34435C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620125 | |||||||
chr18:35620176 | C | G | 1 | a0001c0001t0004g0147 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-103-34384C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620176 | |||||||
chr18:35620480 | TA | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-34078delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620480 | ||||||
chr18:35620549 | G | T | 1 | a0001c0001t0003g0251 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-103-34011G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620549 | |||||||
chr18:35620656 | T | C | 1 | a0001c0001t0011g0260 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-103-33904T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620656 | |||||||
chr18:35620659 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-103-33901G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620659 | |||||||
chr18:35620700 | G | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-33860G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620700 | |||||||
chr18:35620781 | C | CTT | 20 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(17): Show |
20 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-103-33767_-103-33 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620781 | ||||||
chr18:35620781 | C | CTTT | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-33768_-103-33 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620781 | ||||||
chr18:35620794 | TG | T | 9 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0009g0151 others(6): Show |
9 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-103-33764delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35620794 | ||||||
chr18:35620795 | G | T | 76 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(73): Show |
86 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.-103-33765G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35620795 | |||||||
chr18:35621011 | T | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-33549T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621011 | |||||||
chr18:35621045 | T | C | 1 | a0001c0001t0004g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-103-33515T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621045 | |||||||
chr18:35621118 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-33442A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621118 | |||||||
chr18:35621184 | AT | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-33365delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35621184 | ||||||
chr18:35621188 | T | A | 1 | a0001c0001t0001g0176 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-103-33372T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621188 | |||||||
chr18:35621197 | G | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-33363G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621197 | |||||||
chr18:35621234 | AGTAGTGG others(319): Show |
A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-33322_-103-32 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35621234 | ||||||
chr18:35621289 | C | T | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0266 others(8): Show |
11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-33271C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621289 | |||||||
chr18:35621318 | A | G | 1 | a0001c0001t0005g0062 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-103-33242A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621318 | |||||||
chr18:35621384 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-33176G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621384 | |||||||
chr18:35621384 | G | C | 1 | a0001c0001t0001g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-103-33176G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621384 | |||||||
chr18:35621692 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-32868A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621692 | |||||||
chr18:35621704 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-32856C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35621704 | |||||||
chr18:35622004 | C | T | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-32556C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622004 | |||||||
chr18:35622195 | T | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-32365T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622195 | |||||||
chr18:35622215 | T | A | 1 | a0001c0001t0009g0154 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-103-32345T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622215 | |||||||
chr18:35622423 | T | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-32137T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622423 | |||||||
chr18:35622455 | T | C | 1 | a0001c0001t0003g0220 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-103-32105T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622455 | |||||||
chr18:35622489 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-32071T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622489 | |||||||
chr18:35622491 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-32069A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622491 | |||||||
chr18:35622496 | CT | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-32061delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35622496 | ||||||
chr18:35622574 | G | A | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-31986G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622574 | |||||||
chr18:35622686 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-31874C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622686 | |||||||
chr18:35622703 | T | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-31857T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622703 | |||||||
chr18:35622722 | T | C | 1 | a0001c0001t0015g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-103-31838T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622722 | |||||||
chr18:35622734 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-31826T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622734 | |||||||
chr18:35622739 | C | T | 3 | a0001c0001t0003g0247 a0001c0001t0003g0248 a0001c0001t0003g0282 |
3 | HG03017.hp1 HG04115.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-103-31821C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622739 | |||||||
chr18:35622762 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-31798T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622762 | |||||||
chr18:35622795 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.-103-31765T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622795 | |||||||
chr18:35622800 | G | C | 2 | a0001c0001t0003g0223 a0001c0001t0003g0249 |
2 | HG00408.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.-103-31760G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622800 | |||||||
chr18:35622854 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-31706G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622854 | |||||||
chr18:35622868 | G | A | 1 | a0001c0001t0011g0254 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-103-31692G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622868 | |||||||
chr18:35622948 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-31612A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35622948 | |||||||
chr18:35623056 | T | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-31504T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623056 | |||||||
chr18:35623079 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-31481A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623079 | |||||||
chr18:35623098 | G | A | 1 | a0001c0001t0006g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-103-31462G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623098 | |||||||
chr18:35623323 | T | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-31237T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623323 | |||||||
chr18:35623325 | C | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-31235C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623325 | |||||||
chr18:35623464 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-31096C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623464 | |||||||
chr18:35623527 | C | T | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-103-31033C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623527 | |||||||
chr18:35623575 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-103-30985A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623575 | |||||||
chr18:35623767 | A | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-30793A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623767 | |||||||
chr18:35623946 | C | T | 1 | a0001c0001t0003g0232 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-103-30614C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623946 | |||||||
chr18:35623947 | G | A | 1 | a0001c0001t0016g0148 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-103-30613G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35623947 | |||||||
chr18:35624188 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-30372T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624188 | |||||||
chr18:35624213 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0229 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103-30347G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624213 | |||||||
chr18:35624396 | A | G | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0173 |
3 | HG01192.hp2 HG02683.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-103-30164A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624396 | |||||||
chr18:35624467 | C | T | 1 | a0001c0001t0005g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-103-30093C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624467 | |||||||
chr18:35624847 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-29713C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35624847 | |||||||
chr18:35625018 | C | G | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-29542C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625018 | |||||||
chr18:35625201 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-103-29359G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625201 | |||||||
chr18:35625312 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-103-29248G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625312 | |||||||
chr18:35625340 | A | C | 1 | a0001c0001t0001g0098 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-103-29220A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625340 | |||||||
chr18:35625370 | AC | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-29189delC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625370 | |||||||
chr18:35625561 | A | G | 1 | a0001c0001t0002g0167 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-103-28999A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625561 | |||||||
chr18:35625621 | G | T | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-28939G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625621 | |||||||
chr18:35625629 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-28931T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625629 | |||||||
chr18:35625802 | A | G | 190 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(187): Show |
208 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(205): Show |
intron_variant | MODIFIER | c.-103-28758A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625802 | |||||||
chr18:35625833 | C | G | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-28727C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625833 | |||||||
chr18:35625933 | A | G | 42 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
48 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103-28627A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625933 | |||||||
chr18:35625984 | A | G | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-28576A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35625984 | |||||||
chr18:35626036 | C | T | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-103-28524C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626036 | |||||||
chr18:35626152 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-103-28408G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626152 | |||||||
chr18:35626187 | C | T | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-103-28373C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626187 | |||||||
chr18:35626231 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-28329A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626231 | |||||||
chr18:35626270 | T | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-28290T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626270 | |||||||
chr18:35626539 | C | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-28021C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626539 | |||||||
chr18:35626646 | A | G | 1 | a0001c0001t0004g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-103-27914A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626646 | |||||||
chr18:35626653 | G | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-27907G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626653 | |||||||
chr18:35626672 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-27888T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626672 | |||||||
chr18:35626700 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-27860T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626700 | |||||||
chr18:35626714 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-103-27846C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626714 | |||||||
chr18:35626716 | T | C | 1 | a0001c0001t0001g0180 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.-103-27844T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626716 | |||||||
chr18:35626734 | C | T | 1 | a0001c0001t0001g0057 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-103-27826C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626734 | |||||||
chr18:35626924 | A | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-27636A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626924 | |||||||
chr18:35626952 | C | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-27608C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626952 | |||||||
chr18:35626973 | T | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-27587T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626973 | |||||||
chr18:35626977 | C | T | 1 | a0001c0001t0004g0133 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.-103-27583C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35626977 | |||||||
chr18:35627101 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-27459G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627101 | |||||||
chr18:35627254 | C | A | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-27306C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627254 | |||||||
chr18:35627412 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-103-27148G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627412 | |||||||
chr18:35627587 | G | A | 1 | a0001c0001t0001g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-103-26973G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627587 | |||||||
chr18:35627587 | G | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(23): Show |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.-103-26973G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627587 | |||||||
chr18:35627700 | A | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-26860A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627700 | |||||||
chr18:35627716 | G | A | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-26844G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627716 | |||||||
chr18:35627743 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-26817A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627743 | |||||||
chr18:35627750 | C | CGAGCAT | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-26806_-103-26 others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35627750 | ||||||
chr18:35627839 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-26721C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627839 | |||||||
chr18:35627878 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-26682C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627878 | |||||||
chr18:35627902 | C | T | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-103-26658C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627902 | |||||||
chr18:35627959 | CCTCG | C | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-26597_-103-26 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35627959 | ||||||
chr18:35627968 | T | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-26592T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35627968 | |||||||
chr18:35628006 | C | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-26554C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628006 | |||||||
chr18:35628031 | G | A | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-26529G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628031 | |||||||
chr18:35628043 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-26517G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628043 | |||||||
chr18:35628055 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-26505A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628055 | |||||||
chr18:35628065 | G | T | 1 | a0001c0001t0001g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-103-26495G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628065 | |||||||
chr18:35628077 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-103-26483G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628077 | |||||||
chr18:35628153 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
81 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.-103-26407C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628153 | |||||||
chr18:35628350 | G | T | 3 | a0001c0001t0001g0170 a0001c0001t0001g0217 a0001c0001t0001g0218 |
3 | NA18965.hp2 NA19007.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-103-26210G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628350 | |||||||
chr18:35628410 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-26150A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628410 | |||||||
chr18:35628462 | G | A | 3 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG02486.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.-103-26098G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628462 | |||||||
chr18:35628492 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-26068C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628492 | |||||||
chr18:35628561 | A | G | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.-103-25999A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628561 | |||||||
chr18:35628586 | C | T | 1 | a0001c0001t0003g0250 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-103-25974C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628586 | |||||||
chr18:35628720 | T | A | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-103-25840T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628720 | |||||||
chr18:35628732 | G | T | 1 | a0001c0001t0015g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-103-25828G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628732 | |||||||
chr18:35628770 | A | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-25790A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628770 | |||||||
chr18:35628796 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-25764C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628796 | |||||||
chr18:35628901 | C | T | 2 | a0001c0001t0007g0111 a0001c0001t0007g0112 |
2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-103-25659C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628901 | |||||||
chr18:35628916 | G | A | 1 | a0001c0001t0001g0186 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.-103-25644G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628916 | |||||||
chr18:35628920 | G | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-25640G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628920 | |||||||
chr18:35628937 | T | C | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(175): Show |
195 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.-103-25623T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35628937 | |||||||
chr18:35629192 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-25368A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629192 | |||||||
chr18:35629198 | A | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-25362A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629198 | |||||||
chr18:35629217 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-25343C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629217 | |||||||
chr18:35629281 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-25279C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629281 | |||||||
chr18:35629282 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-25278A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629282 | |||||||
chr18:35629526 | T | G | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-25034T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629526 | |||||||
chr18:35629532 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 |
6 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-25028C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629532 | |||||||
chr18:35629544 | C | T | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-25016C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629544 | |||||||
chr18:35629548 | C | A | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-25012C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629548 | |||||||
chr18:35629549 | G | A | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-25011G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629549 | |||||||
chr18:35629653 | AT | A | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-24906delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629653 | |||||||
chr18:35629701 | A | G | 1 | a0001c0001t0009g0153 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-103-24859A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629701 | |||||||
chr18:35629759 | C | A | 1 | a0001c0001t0002g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-103-24801C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629759 | |||||||
chr18:35629868 | C | G | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103-24692C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629868 | |||||||
chr18:35629883 | C | T | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-103-24677C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629883 | |||||||
chr18:35629919 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-24641A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629919 | |||||||
chr18:35629944 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-24616T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35629944 | |||||||
chr18:35630006 | T | A | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-24554T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630006 | |||||||
chr18:35630012 | A | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-24548A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630012 | |||||||
chr18:35630129 | CA | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-24430delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630129 | |||||||
chr18:35630269 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-24291C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630269 | |||||||
chr18:35630273 | G | C | 18 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-24287G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630273 | |||||||
chr18:35630372 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-24188C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630372 | |||||||
chr18:35630414 | A | C | 105 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(102): Show |
116 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.-103-24146A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630414 | |||||||
chr18:35630512 | A | G | 2 | a0001c0001t0005g0064 a0001c0001t0008g0231 |
2 | HG02027.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.-103-24048A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630512 | |||||||
chr18:35630623 | G | T | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.-103-23937G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630623 | |||||||
chr18:35630637 | A | G | 2 | a0001c0001t0001g0057 a0001c0001t0001g0065 |
2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.-103-23923A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630637 | |||||||
chr18:35630682 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(10): Show |
16 | HG02055.hp2 HG02280.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.-103-23878G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630682 | |||||||
chr18:35630697 | T | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-23863T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630697 | |||||||
chr18:35630974 | G | A | 1 | a0001c0001t0001g0279 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-103-23586G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35630974 | |||||||
chr18:35631017 | C | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-23543C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631017 | |||||||
chr18:35631093 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-103-23467G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631093 | |||||||
chr18:35631106 | C | T | 1 | a0001c0001t0014g0222 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-103-23454C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631106 | |||||||
chr18:35631133 | A | G | 1 | a0001c0001t0001g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-103-23427A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631133 | |||||||
chr18:35631134 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-103-23426G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631134 | |||||||
chr18:35631150 | A | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-23410A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631150 | |||||||
chr18:35631417 | A | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-23143A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631417 | |||||||
chr18:35631449 | G | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-23111G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631449 | |||||||
chr18:35631491 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-103-23069C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631491 | |||||||
chr18:35631575 | C | G | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-103-22985C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631575 | |||||||
chr18:35631623 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-22937A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631623 | |||||||
chr18:35631677 | T | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-22883T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631677 | |||||||
chr18:35631813 | G | T | 22 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(19): Show |
26 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103-22747G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631813 | |||||||
chr18:35631865 | T | G | 1 | a0001c0004t0001g0163 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-103-22695T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35631865 | |||||||
chr18:35632030 | G | C | 8 | a0001c0001t0001g0127 a0001c0001t0001g0176 a0001c0001t0001g0177 others(5): Show |
8 | HG02055.hp1 HG02896.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.-103-22530G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632030 | |||||||
chr18:35632093 | A | G | 1 | a0001c0003t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-103-22467A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632093 | |||||||
chr18:35632137 | G | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-22423G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632137 | |||||||
chr18:35632217 | G | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-22343G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632217 | |||||||
chr18:35632280 | T | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-22280T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632280 | |||||||
chr18:35632281 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-22279G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632281 | |||||||
chr18:35632336 | T | G | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-103-22224T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632336 | |||||||
chr18:35632363 | T | G | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-103-22197T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632363 | |||||||
chr18:35632392 | A | G | 22 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(19): Show |
26 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103-22168A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632392 | |||||||
chr18:35632398 | C | T | 22 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(19): Show |
26 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(23): Show |
intron_variant | MODIFIER | c.-103-22162C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632398 | |||||||
chr18:35632461 | A | G | 4 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0229 others(1): Show |
5 | HG02630.hp2 HG02723.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103-22099A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632461 | |||||||
chr18:35632470 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-22090A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632470 | |||||||
chr18:35632605 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0097 |
2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-103-21955A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632605 | |||||||
chr18:35632610 | A | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-21950A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632610 | |||||||
chr18:35632685 | A | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-21875A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632685 | |||||||
chr18:35632694 | A | G | 3 | a0001c0001t0003g0232 a0001c0001t0003g0238 a0001c0001t0019g0056 |
3 | HG02300.hp2 NA18977.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.-103-21866A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632694 | |||||||
chr18:35632798 | C | T | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-21762C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632798 | |||||||
chr18:35632816 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-21744A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632816 | |||||||
chr18:35632836 | A | C | 1 | a0001c0001t0001g0234 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-103-21724A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632836 | |||||||
chr18:35632870 | T | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.-103-21690T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632870 | |||||||
chr18:35632894 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-21666A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35632894 | |||||||
chr18:35633074 | G | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-21486G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633074 | |||||||
chr18:35633175 | C | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-21385C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633175 | |||||||
chr18:35633227 | A | G | 1 | a0001c0001t0004g0144 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-103-21333A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633227 | |||||||
chr18:35633356 | G | A | 99 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(96): Show |
110 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(107): Show |
intron_variant | MODIFIER | c.-103-21204G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633356 | |||||||
chr18:35633426 | C | G | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-21134C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633426 | |||||||
chr18:35633438 | A | G | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-21122A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633438 | |||||||
chr18:35633467 | T | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103-21093T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633467 | |||||||
chr18:35633474 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-21086C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633474 | |||||||
chr18:35633513 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-21047G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633513 | |||||||
chr18:35633583 | C | G | 1 | a0001c0001t0005g0110 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-103-20977C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633583 | |||||||
chr18:35633636 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-20924A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633636 | |||||||
chr18:35633643 | T | C | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(32): Show |
intron_variant | MODIFIER | c.-103-20917T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633643 | |||||||
chr18:35633677 | C | A | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-20883C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633677 | |||||||
chr18:35633791 | C | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-20769C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35633791 | |||||||
chr18:35634101 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0003g0275 |
2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-103-20459G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634101 | |||||||
chr18:35634173 | CATTT | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-20385_-103-20 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35634173 | ||||||
chr18:35634258 | G | A | 3 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 |
3 | HG02896.hp1 HG02897.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.-103-20302G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634258 | |||||||
chr18:35634286 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-20274T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634286 | |||||||
chr18:35634346 | A | C | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-20214A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634346 | |||||||
chr18:35634397 | C | T | 1 | a0001c0001t0001g0083 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-103-20163C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634397 | |||||||
chr18:35634457 | C | T | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-20103C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634457 | |||||||
chr18:35634525 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-20035C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634525 | |||||||
chr18:35634546 | G | A | 2 | a0001c0001t0001g0268 a0001c0001t0003g0275 |
2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-103-20014G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634546 | |||||||
chr18:35634587 | A | G | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-19973A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634587 | |||||||
chr18:35634854 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-19706A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634854 | |||||||
chr18:35634944 | A | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-19616A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35634944 | |||||||
chr18:35635050 | C | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-19510C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635050 | |||||||
chr18:35635416 | G | T | 1 | a0001c0001t0002g0030 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-103-19144G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635416 | |||||||
chr18:35635569 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-103-18991C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635569 | |||||||
chr18:35635680 | C | A | 1 | a0001c0001t0003g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-103-18880C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635680 | |||||||
chr18:35635801 | G | C | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-18759G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35635801 | |||||||
chr18:35636014 | T | A | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-18546T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636014 | |||||||
chr18:35636037 | G | A | 2 | a0001c0001t0002g0016 a0001c0001t0002g0017 |
2 | HG00280.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.-103-18523G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636037 | |||||||
chr18:35636128 | C | A | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-18432C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636128 | |||||||
chr18:35636192 | C | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-18368C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636192 | |||||||
chr18:35636438 | GA | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-18116delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636438 | ||||||
chr18:35636449 | C | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-18111C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636449 | |||||||
chr18:35636498 | G | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-18062G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636498 | |||||||
chr18:35636765 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-17795C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636765 | |||||||
chr18:35636783 | G | GT | 49 | a0001c0001t0001g0095 a0001c0001t0001g0096 a0001c0001t0001g0105 others(46): Show |
51 | HG00280.hp1 HG00609.hp1 HG01074.hp1 others(48): Show |
intron_variant | MODIFIER | c.-103-17752dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | ||||||
chr18:35636783 | G | GTT | 8 | a0001c0001t0001g0211 a0001c0001t0002g0018 a0001c0001t0002g0025 others(5): Show |
8 | HG00408.hp1 HG01192.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.-103-17753_-103-17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | ||||||
chr18:35636783 | GT | G | 55 | a0001c0001t0001g0013 a0001c0001t0001g0100 a0001c0001t0001g0116 others(52): Show |
60 | HG00621.hp2 HG00639.hp1 HG01069.hp1 others(57): Show |
intron_variant | MODIFIER | c.-103-17752delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | ||||||
chr18:35636783 | GTT | G | 14 | a0001c0001t0001g0227 a0001c0001t0001g0276 a0001c0001t0001g0277 others(11): Show |
18 | HG01255.hp2 HG01515.hp1 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.-103-17753_-103-17 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | ||||||
chr18:35636783 | GTTTTTTT others(3): Show |
G | 9 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(6): Show |
10 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(7): Show |
intron_variant | MODIFIER | c.-103-17761_-103-17 others(16): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35636783 | ||||||
chr18:35636795 | T | G | 4 | a0001c0001t0006g0157 a0001c0001t0006g0158 a0001c0001t0006g0159 others(1): Show |
4 | HG01358.hp1 HG02647.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-17765T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636795 | |||||||
chr18:35636796 | T | G | 1 | a0001c0001t0006g0156 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-103-17764T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636796 | |||||||
chr18:35636808 | T | C | 1 | a0001c0001t0004g0145 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.-103-17752T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636808 | |||||||
chr18:35636945 | T | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-17615T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636945 | |||||||
chr18:35636975 | C | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-17585C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35636975 | |||||||
chr18:35637017 | T | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-17543T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637017 | |||||||
chr18:35637321 | G | A | 1 | a0001c0001t0017g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-103-17239G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637321 | |||||||
chr18:35637438 | T | G | 1 | a0001c0001t0001g0087 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-103-17122T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637438 | |||||||
chr18:35637473 | T | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-17087T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637473 | |||||||
chr18:35637497 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-17063G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637497 | |||||||
chr18:35637557 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-17003T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637557 | |||||||
chr18:35637602 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0217 |
2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.-103-16958C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637602 | |||||||
chr18:35637658 | G | A | 85 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(82): Show |
95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-103-16902G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637658 | |||||||
chr18:35637674 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-16886G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35637674 | |||||||
chr18:35637766 | TAG | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-16788_-103-16 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35637766 | ||||||
chr18:35638035 | C | T | 1 | a0001c0001t0001g0207 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-103-16525C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638035 | |||||||
chr18:35638046 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-16514T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638046 | |||||||
chr18:35638088 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-16472A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638088 | |||||||
chr18:35638149 | C | T | 1 | a0002c0002t0003g0239 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.-103-16411C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638149 | |||||||
chr18:35638240 | G | A | 1 | a0001c0004t0001g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-103-16320G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638240 | |||||||
chr18:35638380 | G | A | 1 | a0001c0001t0002g0032 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-103-16180G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638380 | |||||||
chr18:35638468 | A | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-16092A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638468 | |||||||
chr18:35638470 | A | C | 1 | a0001c0004t0001g0125 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-103-16090A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638470 | |||||||
chr18:35638518 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-103-16042G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638518 | |||||||
chr18:35638539 | T | TA | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-16020dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35638539 | ||||||
chr18:35638801 | T | C | 36 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(33): Show |
38 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.-103-15759T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638801 | |||||||
chr18:35638890 | C | T | 2 | a0001c0003t0001g0048 a0001c0003t0001g0049 |
2 | HG02896.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.-103-15670C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35638890 | |||||||
chr18:35639017 | C | G | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-103-15543C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639017 | |||||||
chr18:35639086 | A | G | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-15474A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639086 | |||||||
chr18:35639088 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-15472A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639088 | |||||||
chr18:35639100 | A | G | 1 | a0001c0001t0003g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.-103-15460A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639100 | |||||||
chr18:35639129 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-15431G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639129 | |||||||
chr18:35639183 | G | C | 1 | a0001c0001t0001g0077 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-103-15377G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639183 | |||||||
chr18:35639300 | A | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(176): Show |
196 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.-103-15260A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639300 | |||||||
chr18:35639350 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-15210A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639350 | |||||||
chr18:35639361 | A | T | 85 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(82): Show |
95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-103-15199A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639361 | |||||||
chr18:35639428 | A | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-15132A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639428 | |||||||
chr18:35639551 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-15009A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639551 | |||||||
chr18:35639624 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-14936A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639624 | |||||||
chr18:35639650 | G | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-103-14910G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639650 | |||||||
chr18:35639705 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-14855C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639705 | |||||||
chr18:35639800 | C | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14760C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639800 | |||||||
chr18:35639877 | A | AC | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-14681dupC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35639877 | ||||||
chr18:35639889 | C | G | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-103-14671C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639889 | |||||||
chr18:35639922 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(5): Show |
11 | HG02055.hp2 HG02258.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-14638G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639922 | |||||||
chr18:35639957 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-14603C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35639957 | |||||||
chr18:35640039 | C | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-14521C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640039 | |||||||
chr18:35640100 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14460A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640100 | |||||||
chr18:35640107 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14453A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640107 | |||||||
chr18:35640157 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-14403A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640157 | |||||||
chr18:35640254 | T | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-14306T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640254 | |||||||
chr18:35640258 | A | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-14302A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640258 | |||||||
chr18:35640271 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-14289A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640271 | |||||||
chr18:35640366 | T | A | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-103-14194T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640366 | |||||||
chr18:35640371 | G | GTATC | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-14187_-103-14 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35640371 | ||||||
chr18:35640539 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-103-14021T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640539 | |||||||
chr18:35640799 | T | C | 1 | a0001c0001t0003g0220 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-103-13761T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640799 | |||||||
chr18:35640813 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-13747G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640813 | |||||||
chr18:35640823 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-13737C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640823 | |||||||
chr18:35640956 | T | C | 4 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0113 others(1): Show |
5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-13604T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35640956 | |||||||
chr18:35641109 | A | T | 3 | a0001c0001t0012g0129 a0001c0001t0012g0136 a0001c0001t0012g0138 |
3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-103-13451A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641109 | |||||||
chr18:35641281 | C | A | 2 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
2 | HG02886.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-103-13279C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641281 | |||||||
chr18:35641303 | C | T | 2 | a0001c0001t0002g0020 a0001c0001t0002g0021 |
2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-103-13257C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641303 | |||||||
chr18:35641332 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-13228A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641332 | |||||||
chr18:35641336 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-103-13224C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641336 | |||||||
chr18:35641381 | CT | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-13177delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35641381 | ||||||
chr18:35641717 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-103-12843C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641717 | |||||||
chr18:35641726 | A | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-12834A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641726 | |||||||
chr18:35641831 | C | T | 1 | a0001c0001t0001g0181 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-103-12729C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641831 | |||||||
chr18:35641932 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-12628G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35641932 | |||||||
chr18:35642003 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-12557G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642003 | |||||||
chr18:35642357 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-103-12203G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642357 | |||||||
chr18:35642420 | A | T | 5 | a0001c0001t0001g0115 a0001c0001t0001g0255 a0001c0001t0011g0254 others(2): Show |
5 | HG01109.hp1 HG02257.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.-103-12140A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642420 | |||||||
chr18:35642440 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-103-12120T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642440 | |||||||
chr18:35642450 | G | T | 17 | a0001c0001t0004g0001 a0001c0001t0004g0128 a0001c0001t0004g0130 others(14): Show |
21 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.-103-12110G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642450 | |||||||
chr18:35642581 | T | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-11979T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642581 | |||||||
chr18:35642704 | T | G | 105 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(102): Show |
116 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.-103-11856T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642704 | |||||||
chr18:35642715 | CA | C | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.-103-11844delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642715 | |||||||
chr18:35642716 | AG | A | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11843delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642716 | |||||||
chr18:35642764 | C | T | 53 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0170 others(50): Show |
56 | HG00140.hp1 HG00280.hp2 HG00558.hp2 others(53): Show |
intron_variant | MODIFIER | c.-103-11796C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642764 | |||||||
chr18:35642894 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11666G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642894 | |||||||
chr18:35642905 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11655G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642905 | |||||||
chr18:35642962 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11598G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35642962 | |||||||
chr18:35643034 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-103-11526G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643034 | |||||||
chr18:35643055 | T | C | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-11505T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643055 | |||||||
chr18:35643094 | C | G | 1 | a0001c0001t0006g0184 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-103-11466C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643094 | |||||||
chr18:35643130 | C | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-11430C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643130 | |||||||
chr18:35643237 | G | C | 1 | a0001c0001t0001g0103 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-103-11323G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643237 | |||||||
chr18:35643245 | C | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-11315C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643245 | |||||||
chr18:35643284 | C | T | 1 | a0001c0001t0005g0064 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-103-11276C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643284 | |||||||
chr18:35643434 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-11126G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643434 | |||||||
chr18:35643492 | G | A | 3 | a0001c0001t0010g0011 a0001c0001t0010g0188 a0001c0001t0010g0189 |
4 | HG02735.hp2 HG03017.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-11068G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643492 | |||||||
chr18:35643501 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-11059C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643501 | |||||||
chr18:35643763 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-10797A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643763 | |||||||
chr18:35643795 | C | CA | 42 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
48 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.-103-10752dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35643795 | ||||||
chr18:35643809 | G | A | 1 | a0001c0001t0002g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-103-10751G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643809 | |||||||
chr18:35643809 | G | GA | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-10742dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35643809 | ||||||
chr18:35643810 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-103-10750A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643810 | |||||||
chr18:35643888 | G | C | 1 | a0001c0001t0001g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-103-10672G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643888 | |||||||
chr18:35643920 | G | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-10640G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35643920 | |||||||
chr18:35644067 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-10493G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644067 | |||||||
chr18:35644076 | A | C | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-10484A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644076 | |||||||
chr18:35644334 | C | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-10226C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644334 | |||||||
chr18:35644420 | A | G | 63 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(60): Show |
69 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.-103-10140A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644420 | |||||||
chr18:35644450 | G | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-10110G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644450 | |||||||
chr18:35644666 | T | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-9894T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644666 | |||||||
chr18:35644687 | G | A | 1 | a0001c0001t0004g0150 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-103-9873G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644687 | |||||||
chr18:35644933 | G | T | 1 | a0001c0001t0002g0018 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-103-9627G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644933 | |||||||
chr18:35644935 | G | T | 1 | a0001c0001t0010g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-103-9625G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644935 | |||||||
chr18:35644975 | A | G | 2 | a0001c0001t0001g0087 a0001c0001t0001g0097 |
2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.-103-9585A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35644975 | |||||||
chr18:35645012 | GAATA | G | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-9532_-103-952 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645012 | ||||||
chr18:35645164 | T | A | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-103-9396T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645164 | |||||||
chr18:35645218 | G | GT | 39 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0012 others(36): Show |
41 | HG00140.hp1 HG00408.hp2 HG01069.hp1 others(38): Show |
intron_variant | MODIFIER | c.-103-9316dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645218 | ||||||
chr18:35645218 | G | GTT | 7 | a0001c0001t0001g0216 a0001c0001t0001g0226 a0001c0001t0002g0165 others(4): Show |
7 | HG01978.hp1 HG02486.hp1 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103-9317_-103-931 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645218 | ||||||
chr18:35645218 | GT | G | 106 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(103): Show |
109 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-103-9316delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35645218 | ||||||
chr18:35645224 | T | G | 3 | a0001c0001t0001g0116 a0001c0001t0007g0088 a0001c0001t0007g0107 |
3 | HG02280.hp1 HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.-103-9336T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645224 | |||||||
chr18:35645230 | T | G | 2 | a0001c0001t0001g0268 a0001c0001t0003g0275 |
2 | NA18946.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.-103-9330T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645230 | |||||||
chr18:35645240 | T | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-9320T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645240 | |||||||
chr18:35645291 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-9269C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645291 | |||||||
chr18:35645304 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-9256C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645304 | |||||||
chr18:35645331 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-103-9229A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645331 | |||||||
chr18:35645423 | C | T | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-9137C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645423 | |||||||
chr18:35645516 | T | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-9044T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645516 | |||||||
chr18:35645523 | C | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-9037C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645523 | |||||||
chr18:35645559 | A | T | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-9001A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645559 | |||||||
chr18:35645759 | T | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-8801T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645759 | |||||||
chr18:35645959 | G | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-8601G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645959 | |||||||
chr18:35645978 | G | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-8582G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35645978 | |||||||
chr18:35646140 | A | C | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-103-8420A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646140 | |||||||
chr18:35646149 | T | C | 1 | a0001c0001t0001g0077 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-103-8411T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646149 | |||||||
chr18:35646316 | C | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-8244C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646316 | |||||||
chr18:35646345 | C | T | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-103-8215C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646345 | |||||||
chr18:35646378 | A | G | 4 | a0001c0001t0004g0139 a0001c0001t0012g0129 a0001c0001t0012g0136 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-103-8182A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646378 | |||||||
chr18:35646529 | T | C | 1 | a0001c0001t0002g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-103-8031T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646529 | |||||||
chr18:35646958 | A | G | 10 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.-103-7602A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35646958 | |||||||
chr18:35647245 | G | A | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.-103-7315G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647245 | |||||||
chr18:35647383 | C | T | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-7177C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647383 | |||||||
chr18:35647451 | A | ATTGT | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-7106_-103-710 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35647451 | ||||||
chr18:35647519 | T | C | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-7041T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647519 | |||||||
chr18:35647522 | A | T | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-7038A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647522 | |||||||
chr18:35647523 | T | A | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.-103-7037T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647523 | |||||||
chr18:35647617 | T | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-6943T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647617 | |||||||
chr18:35647636 | T | A | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-6924T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647636 | |||||||
chr18:35647839 | C | T | 1 | a0001c0001t0017g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-103-6721C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647839 | |||||||
chr18:35647917 | C | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-6643C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647917 | |||||||
chr18:35647917 | C | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-6643C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647917 | |||||||
chr18:35647947 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-6613C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647947 | |||||||
chr18:35647948 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-6612G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647948 | |||||||
chr18:35647949 | T | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-6611T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647949 | |||||||
chr18:35647954 | G | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.-103-6606G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35647954 | |||||||
chr18:35648024 | G | GAGA | 9 | a0001c0001t0001g0105 a0001c0001t0001g0119 a0001c0001t0002g0165 others(6): Show |
9 | HG01175.hp2 HG01515.hp1 HG01516.hp1 others(6): Show |
intron_variant | MODIFIER | c.-103-6512_-103-651 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648024 | ||||||
chr18:35648024 | GAGA | G | 39 | a0001c0001t0001g0127 a0001c0001t0004g0001 a0001c0001t0004g0128 others(36): Show |
43 | HG00621.hp2 HG01069.hp1 HG01071.hp1 others(40): Show |
intron_variant | MODIFIER | c.-103-6512_-103-651 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648024 | ||||||
chr18:35648048 | AAGGAAGG others(9): Show |
A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-6487_-103-647 others(20): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648048 | ||||||
chr18:35648057 | A | T | 1 | a0001c0001t0001g0183 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-103-6503A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648057 | |||||||
chr18:35648135 | G | T | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0266 others(8): Show |
11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-103-6425G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648135 | |||||||
chr18:35648137 | AAGGG | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0077 a0001c0001t0016g0148 |
3 | HG02109.hp2 NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-103-6408_-103-640 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648137 | ||||||
chr18:35648184 | T | G | 1 | a0001c0001t0001g0201 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-103-6376T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648184 | |||||||
chr18:35648235 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-6325A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648235 | |||||||
chr18:35648240 | A | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01074.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-103-6320A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648240 | |||||||
chr18:35648295 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-6265T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648295 | |||||||
chr18:35648356 | G | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-6204G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648356 | |||||||
chr18:35648371 | G | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0090 a0001c0001t0001g0094 |
3 | HG01071.hp2 HG01099.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-103-6189G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648371 | |||||||
chr18:35648568 | C | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-5992C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648568 | |||||||
chr18:35648636 | T | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-5924T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648636 | |||||||
chr18:35648742 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-5818A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648742 | |||||||
chr18:35648791 | G | T | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-5769G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648791 | |||||||
chr18:35648801 | A | G | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.-103-5759A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648801 | |||||||
chr18:35648803 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-5757A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648803 | |||||||
chr18:35648809 | G | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0113 others(1): Show |
5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-5751G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648809 | |||||||
chr18:35648840 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.-103-5720G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648840 | |||||||
chr18:35648903 | C | CT | 10 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-103-5655dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35648903 | ||||||
chr18:35648913 | G | A | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-5647G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648913 | |||||||
chr18:35648915 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-103-5645T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35648915 | |||||||
chr18:35649169 | T | C | 1 | a0001c0001t0001g0198 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.-103-5391T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649169 | |||||||
chr18:35649252 | T | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-5308T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649252 | |||||||
chr18:35649351 | G | A | 1 | a0001c0001t0006g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-103-5209G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649351 | |||||||
chr18:35649362 | A | G | 1 | a0001c0001t0001g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-103-5198A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649362 | |||||||
chr18:35649396 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-5164G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649396 | |||||||
chr18:35649444 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-103-5116C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649444 | |||||||
chr18:35649601 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-4959G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649601 | |||||||
chr18:35649654 | A | G | 31 | a0001c0001t0001g0008 a0001c0001t0001g0053 a0001c0001t0001g0054 others(28): Show |
32 | HG00140.hp2 HG00642.hp2 HG01071.hp2 others(29): Show |
intron_variant | MODIFIER | c.-103-4906A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649654 | |||||||
chr18:35649710 | A | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-4850A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649710 | |||||||
chr18:35649852 | T | C | 3 | a0001c0001t0002g0024 a0001c0001t0002g0025 a0001c0001t0002g0026 |
3 | HG01074.hp1 HG01192.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.-103-4708T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649852 | |||||||
chr18:35649967 | C | T | 2 | a0001c0001t0003g0245 a0001c0001t0003g0257 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.-103-4593C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649967 | |||||||
chr18:35649997 | T | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-4563T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35649997 | |||||||
chr18:35650012 | T | A | 3 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 |
3 | NA18946.hp1 NA18986.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.-103-4548T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650012 | |||||||
chr18:35650082 | T | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-4478T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650082 | |||||||
chr18:35650204 | G | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-4356G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650204 | |||||||
chr18:35650226 | C | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-4334C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650226 | |||||||
chr18:35650227 | G | A | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-4333G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650227 | |||||||
chr18:35650370 | G | A | 1 | a0001c0001t0001g0182 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.-103-4190G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650370 | |||||||
chr18:35650388 | C | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-4172C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650388 | |||||||
chr18:35650509 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-103-4051G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650509 | |||||||
chr18:35650514 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-4046A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650514 | |||||||
chr18:35650571 | A | G | 176 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(173): Show |
193 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(190): Show |
intron_variant | MODIFIER | c.-103-3989A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650571 | |||||||
chr18:35650596 | G | C | 1 | a0001c0001t0005g0059 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-103-3964G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650596 | |||||||
chr18:35650621 | C | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(281): Show |
307 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(304): Show |
intron_variant | MODIFIER | c.-103-3939C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650621 | |||||||
chr18:35650626 | C | G | 2 | a0001c0001t0003g0236 a0001c0001t0003g0244 |
2 | NA18948.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-103-3934C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650626 | |||||||
chr18:35650658 | A | C | 1 | a0001c0001t0001g0092 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-103-3902A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650658 | |||||||
chr18:35650854 | C | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.-103-3706C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650854 | |||||||
chr18:35650868 | C | G | 2 | a0001c0001t0001g0203 a0001c0001t0001g0204 |
2 | HG01243.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-103-3692C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650868 | |||||||
chr18:35650872 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-3688C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650872 | |||||||
chr18:35650876 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-3684G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650876 | |||||||
chr18:35650877 | C | T | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-3683C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650877 | |||||||
chr18:35650955 | T | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-3605T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650955 | |||||||
chr18:35650981 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-3579T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35650981 | |||||||
chr18:35651084 | A | G | 1 | a0001c0001t0002g0027 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-103-3476A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651084 | |||||||
chr18:35651104 | C | T | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-3456C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651104 | |||||||
chr18:35651109 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-103-3451G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651109 | |||||||
chr18:35651199 | T | G | 1 | a0001c0001t0007g0111 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-103-3361T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651199 | |||||||
chr18:35651239 | A | G | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.-103-3321A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651239 | |||||||
chr18:35651315 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-103-3245A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651315 | |||||||
chr18:35651356 | C | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-103-3204C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651356 | |||||||
chr18:35651661 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-103-2899A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651661 | |||||||
chr18:35651682 | G | A | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-103-2878G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651682 | |||||||
chr18:35651686 | G | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-103-2874G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651686 | |||||||
chr18:35651726 | A | C | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-103-2834A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651726 | |||||||
chr18:35651751 | G | A | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-2809G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651751 | |||||||
chr18:35651795 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-103-2765A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651795 | |||||||
chr18:35651805 | G | A | 85 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(82): Show |
95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.-103-2755G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651805 | |||||||
chr18:35651826 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG00639.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-103-2734A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651826 | |||||||
chr18:35651965 | C | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.-103-2595C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651965 | |||||||
chr18:35651985 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-103-2575C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35651985 | |||||||
chr18:35652025 | CT | C | 12 | a0001c0001t0001g0127 a0001c0001t0001g0208 a0001c0001t0003g0247 others(9): Show |
12 | HG01069.hp1 HG01071.hp1 HG02015.hp2 others(9): Show |
intron_variant | MODIFIER | c.-103-2524delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35652025 | ||||||
chr18:35652115 | G | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-2445G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652115 | |||||||
chr18:35652120 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-2440T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652120 | |||||||
chr18:35652255 | C | T | 1 | a0001c0001t0007g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-103-2305C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652255 | |||||||
chr18:35652256 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-2304G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652256 | |||||||
chr18:35652282 | TTCTTTCT others(8): Show |
T | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-103-2275_-103-226 others(19): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr18 | 35652282 | ||||||
chr18:35652626 | T | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.-103-1934T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652626 | |||||||
chr18:35652888 | G | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-1672G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652888 | |||||||
chr18:35652912 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-1648A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652912 | |||||||
chr18:35652913 | T | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.-103-1647T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652913 | |||||||
chr18:35652945 | C | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.-103-1615C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652945 | |||||||
chr18:35652991 | A | G | 4 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
7 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.-103-1569A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35652991 | |||||||
chr18:35653110 | T | A | 1 | a0001c0001t0002g0026 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-103-1450T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653110 | |||||||
chr18:35653155 | G | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-103-1405G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653155 | |||||||
chr18:35653158 | G | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-103-1402G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653158 | |||||||
chr18:35653210 | G | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 |
6 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.-103-1350G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653210 | |||||||
chr18:35653375 | C | A | 1 | a0001c0001t0001g0269 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-103-1185C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653375 | |||||||
chr18:35653560 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-1000T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653560 | |||||||
chr18:35653572 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-103-988A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653572 | |||||||
chr18:35653694 | C | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-866C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653694 | |||||||
chr18:35653695 | G | A | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-103-865G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653695 | |||||||
chr18:35653908 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-103-652C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35653908 | |||||||
chr18:35654108 | T | C | 35 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(32): Show |
39 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.-103-452T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654108 | |||||||
chr18:35654196 | T | C | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-103-364T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654196 | |||||||
chr18:35654299 | T | A | 1 | a0001c0001t0004g0128 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-103-261T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654299 | |||||||
chr18:35654454 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-103-106T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654454 | |||||||
chr18:35654474 | AT | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.-103-85delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654474 | |||||||
chr18:35654556 | A | G | 1 | a0001c0001t0002g0016 | 1 | HG02738.hp1 | splice_region_variant&intron_variant | LOW | c.-103-4A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 1/11 | chr18 | 35654556 | |||||||
chr18:35654920 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.139+119G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35654920 | |||||||
chr18:35654969 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.139+168G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35654969 | |||||||
chr18:35655012 | T | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.139+211T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655012 | |||||||
chr18:35655017 | G | A | 1 | a0001c0001t0001g0215 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.139+216G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655017 | |||||||
chr18:35655080 | A | G | 3 | a0001c0001t0011g0254 a0001c0001t0011g0256 a0001c0001t0011g0260 |
3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.139+279A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655080 | |||||||
chr18:35655149 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+348A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655149 | |||||||
chr18:35655353 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.139+552A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655353 | |||||||
chr18:35655499 | C | CT | 14 | a0001c0001t0001g0120 a0001c0001t0001g0127 a0001c0001t0002g0029 others(11): Show |
14 | HG01255.hp2 HG01358.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.139+713dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35655499 | ||||||
chr18:35655839 | C | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+1038C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35655839 | |||||||
chr18:35656103 | C | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.139+1302C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656103 | |||||||
chr18:35656185 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139+1384A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656185 | |||||||
chr18:35656492 | G | GT | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+1692dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35656492 | ||||||
chr18:35656547 | C | T | 3 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 |
3 | HG02486.hp2 HG02809.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.139+1746C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656547 | |||||||
chr18:35656656 | G | C | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.139+1855G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656656 | |||||||
chr18:35656679 | C | T | 1 | a0001c0001t0003g0004 | 3 | NA18939.hp1 NA18951.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.139+1878C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656679 | |||||||
chr18:35656736 | C | A | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.139+1935C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656736 | |||||||
chr18:35656797 | G | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.139+1996G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656797 | |||||||
chr18:35656848 | G | A | 2 | a0001c0001t0001g0217 a0001c0001t0005g0110 |
2 | NA18965.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.139+2047G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656848 | |||||||
chr18:35656872 | A | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.139+2071A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35656872 | |||||||
chr18:35657037 | C | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(23): Show |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.139+2236C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657037 | |||||||
chr18:35657075 | A | AT | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.139+2284dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35657075 | ||||||
chr18:35657322 | G | T | 2 | a0001c0001t0013g0162 a0001c0004t0001g0163 |
2 | HG01884.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.139+2521G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657322 | |||||||
chr18:35657429 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+2628C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657429 | |||||||
chr18:35657535 | A | G | 1 | a0001c0001t0002g0039 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.139+2734A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657535 | |||||||
chr18:35657536 | C | A | 1 | a0001c0001t0002g0039 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.139+2735C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657536 | |||||||
chr18:35657809 | C | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.139+3008C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657809 | |||||||
chr18:35657848 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.139+3047C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657848 | |||||||
chr18:35657849 | G | A | 2 | a0001c0001t0001g0199 a0001c0001t0001g0212 |
2 | HG03927.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.139+3048G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657849 | |||||||
chr18:35657875 | G | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3074G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657875 | |||||||
chr18:35657940 | G | A | 6 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.139+3139G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35657940 | |||||||
chr18:35658081 | A | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0077 |
2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.139+3280A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658081 | |||||||
chr18:35658095 | A | G | 4 | a0001c0001t0001g0268 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG00609.hp2 NA18946.hp2 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.139+3294A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658095 | |||||||
chr18:35658129 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.139+3328A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658129 | |||||||
chr18:35658130 | G | T | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.139+3329G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658130 | |||||||
chr18:35658131 | T | A | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.139+3330T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658131 | |||||||
chr18:35658351 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.139+3550C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658351 | |||||||
chr18:35658360 | A | C | 3 | a0001c0001t0011g0254 a0001c0001t0011g0256 a0001c0001t0011g0260 |
3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.139+3559A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658360 | |||||||
chr18:35658432 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.139+3631A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658432 | |||||||
chr18:35658433 | A | AGGGAAGA others(9): Show |
1 | a0001c0001t0015g0023 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.139+3640_139+3655d others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35658433 | ||||||
chr18:35658585 | T | C | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.139+3784T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658585 | |||||||
chr18:35658627 | G | A | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.139+3826G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658627 | |||||||
chr18:35658709 | C | CT | 8 | a0001c0001t0001g0094 a0001c0001t0001g0100 a0001c0001t0001g0101 others(5): Show |
8 | HG00642.hp2 HG01099.hp1 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.139+3925dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35658709 | ||||||
chr18:35658709 | CT | C | 7 | a0001c0001t0001g0187 a0001c0001t0001g0217 a0001c0001t0001g0276 others(4): Show |
7 | HG01884.hp2 HG01891.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.139+3925delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35658709 | ||||||
chr18:35658795 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.139+3994C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658795 | |||||||
chr18:35658980 | G | T | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.139+4179G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35658980 | |||||||
chr18:35659033 | C | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.139+4232C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659033 | |||||||
chr18:35659501 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.140-4127G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659501 | |||||||
chr18:35659787 | T | C | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.140-3841T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659787 | |||||||
chr18:35659859 | G | A | 2 | a0001c0001t0003g0247 a0001c0001t0003g0248 |
2 | HG03017.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.140-3769G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659859 | |||||||
chr18:35659920 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.140-3708A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659920 | |||||||
chr18:35659963 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.140-3665G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35659963 | |||||||
chr18:35660231 | A | ACTTTATA others(3): Show |
180 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(177): Show |
197 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(194): Show |
intron_variant | MODIFIER | c.140-3392_140-3391i others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35660231 | ||||||
chr18:35660235 | T | C | 1 | a0001c0001t0001g0113 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.140-3393T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660235 | |||||||
chr18:35660237 | G | T | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.140-3391G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660237 | |||||||
chr18:35660262 | A | G | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.140-3366A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660262 | |||||||
chr18:35660551 | T | A | 1 | a0001c0001t0001g0174 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.140-3077T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660551 | |||||||
chr18:35660607 | T | A | 2 | a0001c0001t0003g0245 a0001c0001t0003g0257 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.140-3021T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660607 | |||||||
chr18:35660632 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.140-2996C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660632 | |||||||
chr18:35660684 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2944A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660684 | |||||||
chr18:35660834 | G | A | 13 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(10): Show |
14 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(11): Show |
intron_variant | MODIFIER | c.140-2794G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660834 | |||||||
chr18:35660853 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.140-2775A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35660853 | |||||||
chr18:35661201 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.140-2427G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661201 | |||||||
chr18:35661370 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.140-2258G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661370 | |||||||
chr18:35661415 | G | T | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-2213G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661415 | |||||||
chr18:35661510 | A | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2118A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661510 | |||||||
chr18:35661511 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2117T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661511 | |||||||
chr18:35661512 | C | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2116C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661512 | |||||||
chr18:35661512 | C | CAA | 6 | a0001c0001t0002g0002 a0001c0001t0002g0021 a0001c0001t0002g0161 others(3): Show |
10 | HG01168.hp1 HG02257.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.140-2105_140-2104d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35661512 | ||||||
chr18:35661512 | C | CAAA | 35 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(32): Show |
37 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(34): Show |
intron_variant | MODIFIER | c.140-2106_140-2104d others(5): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35661512 | ||||||
chr18:35661598 | CTT | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-2028_140-2027d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35661598 | ||||||
chr18:35661636 | T | C | 36 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(33): Show |
40 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.140-1992T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661636 | |||||||
chr18:35661653 | G | A | 2 | a0001c0001t0001g0276 a0001c0001t0001g0277 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.140-1975G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661653 | |||||||
chr18:35661744 | T | C | 1 | a0001c0001t0001g0233 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.140-1884T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35661744 | |||||||
chr18:35662010 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.140-1618G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662010 | |||||||
chr18:35662107 | A | T | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-1521A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662107 | |||||||
chr18:35662148 | A | ATT | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.140-1479_140-1478d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662148 | ||||||
chr18:35662506 | G | GCT | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-1121_140-1120d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662506 | ||||||
chr18:35662582 | TG | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.140-1044delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662582 | ||||||
chr18:35662609 | AT | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.140-1013delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35662609 | ||||||
chr18:35662750 | G | T | 4 | a0001c0001t0001g0074 a0001c0001t0001g0090 a0001c0001t0001g0092 others(1): Show |
4 | HG01071.hp2 HG01099.hp1 HG01106.hp1 others(1): Show |
intron_variant | MODIFIER | c.140-878G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662750 | |||||||
chr18:35662884 | G | A | 6 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.140-744G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35662884 | |||||||
chr18:35663069 | A | G | 1 | a0001c0001t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.140-559A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663069 | |||||||
chr18:35663121 | G | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.140-507G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663121 | |||||||
chr18:35663131 | G | A | 1 | a0001c0001t0004g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.140-497G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663131 | |||||||
chr18:35663308 | GGACTCTA | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.140-318_140-312del others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr18 | 35663308 | ||||||
chr18:35663345 | C | T | 1 | a0001c0001t0001g0204 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.140-283C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663345 | |||||||
chr18:35663350 | T | C | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.140-278T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663350 | |||||||
chr18:35663448 | C | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.140-180C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663448 | |||||||
chr18:35663477 | C | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.140-151C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663477 | |||||||
chr18:35663572 | A | G | 100 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(97): Show |
111 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.140-56A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 2/11 | chr18 | 35663572 | |||||||
chr18:35664064 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.314+262A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664064 | |||||||
chr18:35664317 | CTT | C | 6 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+519_314+520del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35664317 | ||||||
chr18:35664561 | A | G | 36 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(33): Show |
40 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.314+759A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664561 | |||||||
chr18:35664651 | T | C | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+849T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664651 | |||||||
chr18:35664832 | A | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0065 |
2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.314+1030A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664832 | |||||||
chr18:35664836 | A | T | 1 | a0001c0001t0001g0012 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.314+1034A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664836 | |||||||
chr18:35664933 | A | G | 16 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(13): Show |
16 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.314+1131A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664933 | |||||||
chr18:35664950 | G | C | 1 | a0001c0001t0001g0196 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.314+1148G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664950 | |||||||
chr18:35664964 | A | T | 1 | a0001c0001t0001g0118 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+1162A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664964 | |||||||
chr18:35664966 | A | C | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.314+1164A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35664966 | |||||||
chr18:35665270 | T | C | 2 | a0001c0001t0001g0058 a0001c0001t0001g0077 |
2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.314+1468T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665270 | |||||||
chr18:35665422 | G | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.314+1620G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665422 | |||||||
chr18:35665436 | G | A | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1634G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665436 | |||||||
chr18:35665479 | C | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1677C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665479 | |||||||
chr18:35665536 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.314+1734A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665536 | |||||||
chr18:35665593 | G | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.314+1791G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665593 | |||||||
chr18:35665595 | A | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.314+1793A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665595 | |||||||
chr18:35665595 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314+1793A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665595 | |||||||
chr18:35665699 | G | A | 2 | a0001c0001t0001g0057 a0001c0001t0001g0065 |
2 | HG01358.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.314+1897G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665699 | |||||||
chr18:35665985 | G | A | 1 | a0001c0001t0003g0238 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.314+2183G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35665985 | |||||||
chr18:35666002 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+2200A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666002 | |||||||
chr18:35666106 | T | G | 1 | a0001c0001t0001g0272 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.314+2304T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666106 | |||||||
chr18:35666174 | C | G | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+2372C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666174 | |||||||
chr18:35666322 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.314+2520G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666322 | |||||||
chr18:35666494 | A | G | 1 | a0001c0001t0002g0022 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.314+2692A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666494 | |||||||
chr18:35666919 | C | CT | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.314+3118dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35666919 | ||||||
chr18:35666938 | CT | C | 7 | a0001c0001t0002g0021 a0001c0001t0002g0165 a0001c0001t0002g0166 others(4): Show |
7 | HG01168.hp1 HG01884.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.314+3142delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35666938 | ||||||
chr18:35666944 | T | A | 37 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(34): Show |
43 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.314+3142T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35666944 | |||||||
chr18:35667186 | TG | T | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0266 others(8): Show |
11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.314+3386delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35667186 | ||||||
chr18:35667210 | C | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0055 a0001c0001t0001g0075 |
4 | HG01257.hp2 HG01258.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+3408C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667210 | |||||||
chr18:35667266 | G | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+3464G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667266 | |||||||
chr18:35667570 | T | C | 10 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+3768T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667570 | |||||||
chr18:35667571 | A | G | 1 | a0001c0001t0008g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.314+3769A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667571 | |||||||
chr18:35667633 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.314+3831A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667633 | |||||||
chr18:35667681 | T | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3879T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667681 | |||||||
chr18:35667708 | G | A | 11 | a0001c0001t0005g0007 a0001c0001t0005g0059 a0001c0001t0005g0062 others(8): Show |
12 | HG02027.hp1 HG02074.hp1 NA18747.hp1 others(9): Show |
intron_variant | MODIFIER | c.314+3906G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667708 | |||||||
chr18:35667919 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.314+4117A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35667919 | |||||||
chr18:35668052 | T | A | 1 | a0001c0001t0001g0210 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.314+4250T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668052 | |||||||
chr18:35668167 | A | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.314+4365A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668167 | |||||||
chr18:35668295 | G | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0226 others(7): Show |
11 | HG01884.hp1 HG02630.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+4493G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668295 | |||||||
chr18:35668640 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+4838T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668640 | |||||||
chr18:35668798 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.314+4996G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668798 | |||||||
chr18:35668968 | G | A | 3 | a0001c0001t0002g0037 a0001c0001t0002g0039 a0001c0001t0018g0033 |
3 | HG00408.hp1 HG00609.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.314+5166G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35668968 | |||||||
chr18:35669018 | G | A | 3 | a0001c0001t0001g0252 a0001c0001t0002g0002 a0001c0001t0002g0161 |
7 | HG01106.hp2 HG02258.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+5216G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669018 | |||||||
chr18:35669109 | C | T | 18 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+5307C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669109 | |||||||
chr18:35669112 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+5310G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669112 | |||||||
chr18:35669123 | C | T | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG01106.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.314+5321C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669123 | |||||||
chr18:35669206 | A | T | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.314+5404A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669206 | |||||||
chr18:35669231 | A | ACT | 283 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(280): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.314+5430_314+5431i others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35669231 | ||||||
chr18:35669319 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.314+5517C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669319 | |||||||
chr18:35669335 | A | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.314+5533A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669335 | |||||||
chr18:35669424 | G | A | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.314+5622G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669424 | |||||||
chr18:35669479 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+5677A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669479 | |||||||
chr18:35669573 | G | A | 2 | a0001c0001t0003g0223 a0001c0001t0003g0249 |
2 | HG00408.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.314+5771G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669573 | |||||||
chr18:35669606 | A | T | 3 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 |
3 | HG01515.hp1 HG01516.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.314+5804A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669606 | |||||||
chr18:35669638 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+5836A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669638 | |||||||
chr18:35669724 | A | G | 5 | a0001c0001t0003g0224 a0002c0002t0003g0239 a0002c0002t0003g0241 others(2): Show |
5 | NA18952.hp2 NA18960.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+5922A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669724 | |||||||
chr18:35669874 | G | C | 1 | a0001c0001t0010g0188 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.314+6072G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669874 | |||||||
chr18:35669988 | A | C | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.314+6186A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35669988 | |||||||
chr18:35670011 | C | G | 2 | a0001c0001t0001g0072 a0001c0001t0001g0095 |
2 | HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.314+6209C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670011 | |||||||
chr18:35670094 | A | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0281 |
2 | HG02572.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.314+6292A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670094 | |||||||
chr18:35670101 | G | A | 2 | a0001c0001t0003g0236 a0001c0001t0003g0244 |
2 | NA18948.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.314+6299G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670101 | |||||||
chr18:35670146 | G | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.314+6344G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670146 | |||||||
chr18:35670270 | G | A | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.314+6468G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670270 | |||||||
chr18:35670319 | T | C | 44 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(41): Show |
50 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(47): Show |
intron_variant | MODIFIER | c.314+6517T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670319 | |||||||
chr18:35670320 | A | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+6518A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670320 | |||||||
chr18:35670760 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315-6831A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670760 | |||||||
chr18:35670874 | A | G | 1 | a0001c0001t0002g0042 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.315-6717A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670874 | |||||||
chr18:35670895 | C | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(23): Show |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.315-6696C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670895 | |||||||
chr18:35670941 | T | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.315-6650T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35670941 | |||||||
chr18:35671104 | C | CT | 11 | a0001c0001t0004g0001 a0001c0001t0004g0130 a0001c0001t0004g0134 others(8): Show |
15 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.315-6478dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35671104 | ||||||
chr18:35671195 | G | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.315-6396G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671195 | |||||||
chr18:35671325 | T | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.315-6266T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671325 | |||||||
chr18:35671422 | C | T | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.315-6169C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671422 | |||||||
chr18:35671453 | T | C | 4 | a0001c0001t0004g0139 a0001c0001t0012g0129 a0001c0001t0012g0136 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-6138T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671453 | |||||||
chr18:35671543 | G | A | 27 | a0001c0001t0003g0004 a0001c0001t0003g0220 a0001c0001t0003g0223 others(24): Show |
29 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(26): Show |
intron_variant | MODIFIER | c.315-6048G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671543 | |||||||
chr18:35671828 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-5763A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671828 | |||||||
chr18:35671868 | T | C | 1 | a0001c0001t0007g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.315-5723T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35671868 | |||||||
chr18:35672248 | T | C | 4 | a0001c0001t0001g0003 a0001c0001t0001g0117 a0001c0001t0001g0118 others(1): Show |
7 | HG02647.hp2 HG03098.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-5343T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672248 | |||||||
chr18:35672302 | T | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(16): Show |
20 | HG00609.hp2 HG00639.hp2 HG01069.hp1 others(17): Show |
intron_variant | MODIFIER | c.315-5289T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672302 | |||||||
chr18:35672541 | G | A | 1 | a0001c0001t0002g0028 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.315-5050G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672541 | |||||||
chr18:35672714 | A | G | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-4877A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672714 | |||||||
chr18:35672780 | A | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-4811A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35672780 | |||||||
chr18:35672822 | T | TTTATTGA others(21): Show |
1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.315-4764_315-4737d others(30): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35672822 | ||||||
chr18:35673500 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-4091T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673500 | |||||||
chr18:35673549 | A | G | 1 | a0001c0001t0003g0258 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.315-4042A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673549 | |||||||
chr18:35673642 | T | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.315-3949T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673642 | |||||||
chr18:35673649 | G | T | 1 | a0001c0001t0001g0055 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.315-3942G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673649 | |||||||
chr18:35673969 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-3622T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673969 | |||||||
chr18:35673990 | C | A | 1 | a0001c0001t0001g0280 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.315-3601C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673990 | |||||||
chr18:35673993 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-3598A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35673993 | |||||||
chr18:35674101 | A | C | 1 | a0001c0001t0001g0173 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.315-3490A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674101 | |||||||
chr18:35674244 | G | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.315-3347G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674244 | |||||||
chr18:35674749 | C | T | 6 | a0001c0001t0003g0235 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2842C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674749 | |||||||
chr18:35674785 | C | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.315-2806C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674785 | |||||||
chr18:35674908 | G | A | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02976.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.315-2683G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674908 | |||||||
chr18:35674944 | C | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315-2647C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674944 | |||||||
chr18:35674973 | A | AC | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2617dupC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674973 | ||||||
chr18:35674975 | T | C | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2616T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35674975 | |||||||
chr18:35674982 | C | CA | 37 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0065 others(34): Show |
37 | HG00280.hp2 HG01106.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.315-2581dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | ||||||
chr18:35674982 | CA | C | 29 | a0001c0001t0001g0054 a0001c0001t0001g0083 a0001c0001t0001g0095 others(26): Show |
30 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.315-2581delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | ||||||
chr18:35674982 | CAA | C | 36 | a0001c0001t0002g0002 a0001c0001t0002g0016 a0001c0001t0002g0019 others(33): Show |
44 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.315-2582_315-2581d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | ||||||
chr18:35674982 | CAAAAAA | C | 6 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(3): Show |
6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-2586_315-2581d others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35674982 | ||||||
chr18:35675008 | AAAG | A | 10 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(7): Show |
11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.315-2582_315-2580d others(5): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675008 | |||||||
chr18:35675050 | A | G | 68 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(65): Show |
71 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(68): Show |
intron_variant | MODIFIER | c.315-2541A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675050 | |||||||
chr18:35675118 | T | C | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.315-2473T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675118 | |||||||
chr18:35675255 | G | T | 1 | a0001c0001t0001g0092 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.315-2336G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675255 | |||||||
chr18:35675259 | G | T | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-2332G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675259 | |||||||
chr18:35675344 | TATTA | T | 3 | a0001c0001t0002g0005 a0001c0001t0002g0030 a0001c0001t0002g0035 |
4 | NA18989.hp2 NA18993.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-2243_315-2240d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35675344 | ||||||
chr18:35675664 | A | G | 5 | a0001c0001t0001g0170 a0001c0001t0001g0175 a0001c0001t0001g0206 others(2): Show |
5 | HG02523.hp1 NA18965.hp2 NA18989.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-1927A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675664 | |||||||
chr18:35675749 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-1842C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675749 | |||||||
chr18:35675896 | T | G | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.315-1695T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675896 | |||||||
chr18:35675980 | A | G | 2 | a0002c0002t0003g0242 a0002c0002t0003g0243 |
2 | NA18952.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.315-1611A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35675980 | |||||||
chr18:35676213 | A | G | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-1378A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676213 | |||||||
chr18:35676268 | TC | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-1321delC | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr18 | 35676268 | ||||||
chr18:35676306 | GA | G | 6 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-1284delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676306 | |||||||
chr18:35676408 | A | C | 3 | a0001c0001t0010g0011 a0001c0001t0010g0188 a0001c0001t0010g0189 |
4 | HG02735.hp2 HG03017.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-1183A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676408 | |||||||
chr18:35676499 | C | T | 1 | a0001c0001t0003g0220 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.315-1092C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676499 | |||||||
chr18:35676517 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.315-1074A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676517 | |||||||
chr18:35676529 | G | C | 75 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(72): Show |
81 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(78): Show |
intron_variant | MODIFIER | c.315-1062G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676529 | |||||||
chr18:35676618 | G | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-973G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676618 | |||||||
chr18:35676929 | T | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-662T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676929 | |||||||
chr18:35676997 | G | A | 38 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(35): Show |
44 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(41): Show |
intron_variant | MODIFIER | c.315-594G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35676997 | |||||||
chr18:35677010 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.315-581A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677010 | |||||||
chr18:35677156 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.315-435C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677156 | |||||||
chr18:35677196 | G | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.315-395G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677196 | |||||||
chr18:35677338 | A | G | 1 | a0001c0001t0003g0209 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.315-253A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677338 | |||||||
chr18:35677417 | A | G | 10 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.315-174A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677417 | |||||||
chr18:35677425 | C | T | 4 | a0001c0001t0004g0139 a0001c0001t0012g0129 a0001c0001t0012g0136 others(1): Show |
4 | HG02895.hp2 HG02897.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-166C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677425 | |||||||
chr18:35677529 | A | G | 1 | a0001c0001t0006g0158 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.315-62A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677529 | |||||||
chr18:35677548 | T | C | 1 | a0001c0001t0001g0175 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.315-43T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 3/11 | chr18 | 35677548 | |||||||
chr18:35677808 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.481+51C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35677808 | |||||||
chr18:35678237 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0181 a0001c0001t0001g0194 |
4 | HG00140.hp1 HG01168.hp2 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.481+480C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678237 | |||||||
chr18:35678306 | T | A | 1 | a0001c0001t0001g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.481+549T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678306 | |||||||
chr18:35678322 | T | A | 1 | a0001c0001t0003g0223 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.481+565T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678322 | |||||||
chr18:35678349 | C | CAT | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.481+592_481+593ins others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678349 | |||||||
chr18:35678350 | G | A | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.481+593G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678350 | |||||||
chr18:35678681 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0106 a0001c0001t0001g0113 others(1): Show |
5 | NA18939.hp2 NA18957.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+924C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35678681 | |||||||
chr18:35678984 | T | TA | 3 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0161 |
7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.481+1228dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35678984 | ||||||
chr18:35679293 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.481+1536G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679293 | |||||||
chr18:35679319 | A | T | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.481+1562A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679319 | |||||||
chr18:35679606 | C | T | 74 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
80 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.481+1849C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679606 | |||||||
chr18:35679673 | C | T | 33 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(30): Show |
35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.481+1916C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679673 | |||||||
chr18:35679689 | G | T | 3 | a0001c0001t0001g0180 a0001c0001t0001g0208 a0001c0001t0003g0209 |
3 | HG02015.hp2 NA18993.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.481+1932G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679689 | |||||||
chr18:35679737 | CT | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.481+1982delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35679737 | ||||||
chr18:35679817 | C | G | 2 | a0001c0001t0006g0184 a0001c0001t0006g0193 |
2 | HG00642.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.481+2060C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679817 | |||||||
chr18:35679915 | A | C | 36 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(33): Show |
38 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.481+2158A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679915 | |||||||
chr18:35679960 | C | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.481+2203C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679960 | |||||||
chr18:35679993 | G | A | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.481+2236G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35679993 | |||||||
chr18:35680207 | C | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.481+2450C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680207 | |||||||
chr18:35680241 | A | G | 1 | a0001c0001t0001g0217 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.481+2484A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680241 | |||||||
chr18:35680266 | T | A | 16 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(13): Show |
16 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(13): Show |
intron_variant | MODIFIER | c.481+2509T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680266 | |||||||
chr18:35680409 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.481+2652C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680409 | |||||||
chr18:35680482 | T | C | 282 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(279): Show |
305 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(302): Show |
intron_variant | MODIFIER | c.481+2725T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680482 | |||||||
chr18:35680802 | A | G | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.482-2589A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35680802 | |||||||
chr18:35681053 | T | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.482-2338T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681053 | |||||||
chr18:35681087 | C | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.482-2304C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681087 | |||||||
chr18:35681329 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482-2062C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681329 | |||||||
chr18:35681427 | G | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.482-1964G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681427 | |||||||
chr18:35681487 | A | AT | 34 | a0001c0001t0001g0013 a0001c0001t0001g0225 a0001c0001t0001g0229 others(31): Show |
39 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.482-1893dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35681487 | ||||||
chr18:35681552 | G | A | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1839G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681552 | |||||||
chr18:35681594 | T | C | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1797T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681594 | |||||||
chr18:35681618 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.482-1773C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681618 | |||||||
chr18:35681928 | C | T | 5 | a0001c0001t0004g0122 a0001c0001t0004g0123 a0001c0001t0004g0124 others(2): Show |
5 | HG01515.hp1 HG01516.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-1463C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35681928 | |||||||
chr18:35682176 | TA | T | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.482-1214delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682176 | |||||||
chr18:35682260 | A | ATTGATTA others(11): Show |
4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1130_482-1129i others(20): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682260 | ||||||
chr18:35682262 | C | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1129C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682262 | |||||||
chr18:35682263 | C | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1128C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682263 | |||||||
chr18:35682264 | C | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.482-1127C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682264 | |||||||
chr18:35682484 | G | A | 1 | a0001c0001t0005g0068 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.482-907G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682484 | |||||||
chr18:35682548 | T | C | 1 | a0001c0001t0002g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.482-843T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682548 | |||||||
chr18:35682565 | G | A | 33 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(30): Show |
35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.482-826G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682565 | |||||||
chr18:35682600 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.482-791A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682600 | |||||||
chr18:35682908 | T | TA | 191 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(188): Show |
203 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.482-462dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | ||||||
chr18:35682908 | T | TAA | 6 | a0001c0001t0001g0190 a0001c0001t0006g0156 a0001c0001t0006g0157 others(3): Show |
6 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.482-463_482-462dup others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | ||||||
chr18:35682908 | TA | T | 34 | a0001c0001t0001g0014 a0001c0001t0002g0165 a0001c0001t0002g0166 others(31): Show |
39 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(36): Show |
intron_variant | MODIFIER | c.482-462delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | ||||||
chr18:35682908 | TAA | T | 37 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(34): Show |
43 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.482-463_482-462del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35682908 | ||||||
chr18:35682982 | G | A | 2 | a0001c0001t0001g0087 a0001c0001t0001g0097 |
2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.482-409G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682982 | |||||||
chr18:35682991 | C | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.482-400C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35682991 | |||||||
chr18:35683111 | CAG | C | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.482-277_482-276del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr18 | 35683111 | ||||||
chr18:35683298 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.482-93G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 4/11 | chr18 | 35683298 | |||||||
chr18:35683827 | G | A | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.689+229G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35683827 | |||||||
chr18:35683961 | T | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.689+363T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35683961 | |||||||
chr18:35684004 | A | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+406A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684004 | |||||||
chr18:35684034 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.689+436G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684034 | |||||||
chr18:35684093 | G | A | 182 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(179): Show |
199 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.689+495G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684093 | |||||||
chr18:35684155 | G | C | 2 | a0001c0001t0012g0136 a0001c0001t0012g0138 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.689+557G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684155 | |||||||
chr18:35684189 | G | C | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.689+591G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684189 | |||||||
chr18:35684221 | G | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+623G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684221 | |||||||
chr18:35684245 | T | TGTTAACA others(5): Show |
49 | a0001c0001t0001g0262 a0001c0001t0002g0002 a0001c0001t0002g0005 others(46): Show |
55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.689+650_689+651ins others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35684245 | ||||||
chr18:35684346 | A | AT | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.689+754dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35684346 | ||||||
chr18:35684393 | C | CCAAT | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.689+800_689+803dup others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35684393 | ||||||
chr18:35684446 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.689+848A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684446 | |||||||
chr18:35684787 | T | G | 1 | a0001c0001t0001g0012 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.689+1189T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35684787 | |||||||
chr18:35685166 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.689+1568A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685166 | |||||||
chr18:35685208 | C | T | 6 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(3): Show |
6 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.689+1610C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685208 | |||||||
chr18:35685229 | C | T | 8 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(5): Show |
8 | HG01069.hp1 HG01071.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+1631C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685229 | |||||||
chr18:35685231 | T | C | 45 | a0001c0001t0001g0262 a0001c0001t0002g0002 a0001c0001t0002g0005 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.689+1633T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685231 | |||||||
chr18:35685234 | A | G | 45 | a0001c0001t0001g0262 a0001c0001t0002g0002 a0001c0001t0002g0005 others(42): Show |
51 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.689+1636A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685234 | |||||||
chr18:35685242 | G | A | 1 | a0001c0001t0003g0282 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.689+1644G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685242 | |||||||
chr18:35685305 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.689+1707C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685305 | |||||||
chr18:35685366 | T | C | 1 | a0001c0001t0001g0171 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.690-1650T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685366 | |||||||
chr18:35685379 | A | G | 1 | a0001c0001t0006g0160 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.690-1637A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685379 | |||||||
chr18:35685381 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-1635A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685381 | |||||||
chr18:35685384 | A | C | 49 | a0001c0001t0001g0262 a0001c0001t0002g0002 a0001c0001t0002g0005 others(46): Show |
55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.690-1632A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685384 | |||||||
chr18:35685455 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.690-1561G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685455 | |||||||
chr18:35685484 | T | TA | 57 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(54): Show |
62 | HG00609.hp2 HG00621.hp2 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.690-1517dupA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35685484 | ||||||
chr18:35685484 | T | TAA | 9 | a0001c0001t0001g0169 a0001c0001t0002g0002 a0001c0001t0002g0045 others(6): Show |
13 | HG01069.hp1 HG01071.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.690-1518_690-1517d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35685484 | ||||||
chr18:35685484 | TA | T | 7 | a0001c0001t0001g0094 a0001c0001t0003g0224 a0001c0001t0006g0156 others(4): Show |
7 | HG01099.hp1 HG01255.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-1517delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35685484 | ||||||
chr18:35685631 | A | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-1385A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685631 | |||||||
chr18:35685832 | C | T | 3 | a0001c0001t0011g0254 a0001c0001t0011g0256 a0001c0001t0011g0260 |
3 | HG01109.hp1 HG02257.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.690-1184C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685832 | |||||||
chr18:35685882 | C | G | 1 | a0001c0001t0001g0206 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.690-1134C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685882 | |||||||
chr18:35685908 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.690-1108A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35685908 | |||||||
chr18:35686038 | A | G | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-978A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686038 | |||||||
chr18:35686112 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.690-904C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686112 | |||||||
chr18:35686114 | TAGAAAAT others(11): Show |
T | 1 | a0001c0001t0004g0141 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.690-895_690-878del others(18): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35686114 | ||||||
chr18:35686128 | C | T | 98 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(95): Show |
109 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(106): Show |
intron_variant | MODIFIER | c.690-888C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686128 | |||||||
chr18:35686233 | GAA | G | 4 | a0001c0001t0001g0262 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-781_690-780del others(2): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr18 | 35686233 | ||||||
chr18:35686235 | A | G | 83 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(80): Show |
93 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.690-781A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686235 | |||||||
chr18:35686350 | C | T | 1 | a0001c0003t0001g0051 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.690-666C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686350 | |||||||
chr18:35686366 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(4): Show |
10 | HG02055.hp2 HG02109.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.690-650A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686366 | |||||||
chr18:35686380 | A | G | 1 | a0001c0001t0020g0052 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.690-636A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686380 | |||||||
chr18:35686499 | A | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-517A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686499 | |||||||
chr18:35686613 | C | T | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.690-403C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686613 | |||||||
chr18:35686619 | C | T | 12 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.690-397C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686619 | |||||||
chr18:35686698 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-318T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686698 | |||||||
chr18:35686735 | C | A | 1 | a0001c0001t0001g0179 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.690-281C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686735 | |||||||
chr18:35686746 | T | A | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.690-270T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686746 | |||||||
chr18:35686924 | A | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.690-92A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686924 | |||||||
chr18:35686981 | T | C | 3 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.690-35T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 5/11 | chr18 | 35686981 | |||||||
chr18:35687294 | C | T | 1 | a0002c0002t0003g0243 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.860+108C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687294 | |||||||
chr18:35687358 | C | T | 1 | a0001c0001t0009g0152 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.860+172C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687358 | |||||||
chr18:35687462 | G | C | 10 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.860+276G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687462 | |||||||
chr18:35687713 | T | C | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.860+527T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687713 | |||||||
chr18:35687917 | T | C | 2 | a0001c0001t0001g0072 a0001c0001t0001g0095 |
2 | HG01256.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.860+731T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687917 | |||||||
chr18:35687977 | T | G | 86 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.860+791T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35687977 | |||||||
chr18:35688199 | G | T | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.861-974G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688199 | |||||||
chr18:35688219 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.861-954A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688219 | |||||||
chr18:35688231 | T | G | 2 | a0001c0001t0001g0058 a0001c0001t0001g0077 |
2 | NA19004.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.861-942T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688231 | |||||||
chr18:35688386 | ATTT | A | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.861-782_861-780del others(3): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 35688386 | ||||||
chr18:35688466 | T | TAAATCTT others(14): Show |
1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.861-706_861-686dup others(21): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr18 | 35688466 | ||||||
chr18:35688578 | T | C | 2 | a0001c0001t0007g0088 a0001c0001t0007g0107 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.861-595T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688578 | |||||||
chr18:35688606 | A | C | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.861-567A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688606 | |||||||
chr18:35688687 | A | G | 4 | a0001c0001t0001g0262 a0001c0001t0002g0165 a0001c0001t0002g0166 others(1): Show |
4 | HG02257.hp2 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.861-486A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688687 | |||||||
chr18:35688736 | C | T | 1 | a0001c0001t0001g0195 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.861-437C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688736 | |||||||
chr18:35688906 | T | C | 1 | a0001c0001t0001g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.861-267T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35688906 | |||||||
chr18:35689145 | C | T | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.861-28C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 6/11 | chr18 | 35689145 | |||||||
chr18:35689303 | A | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(45): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.978+13A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689303 | |||||||
chr18:35689310 | T | A | 85 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(82): Show |
95 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(92): Show |
intron_variant | MODIFIER | c.978+20T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689310 | |||||||
chr18:35689617 | AAAACATA others(12): Show |
A | 32 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0004g0001 others(29): Show |
36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.978+347_978+365del others(19): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 35689617 | ||||||
chr18:35689685 | A | T | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.978+395A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689685 | |||||||
chr18:35689742 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.978+452C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689742 | |||||||
chr18:35689752 | C | T | 1 | a0001c0001t0001g0267 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.978+462C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689752 | |||||||
chr18:35689789 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.978+499A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689789 | |||||||
chr18:35689824 | C | T | 2 | a0001c0001t0001g0170 a0001c0001t0001g0217 |
2 | NA18965.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.978+534C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689824 | |||||||
chr18:35689830 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(67): Show |
80 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.978+540G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689830 | |||||||
chr18:35689979 | T | C | 1 | a0001c0001t0003g0247 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.978+689T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35689979 | |||||||
chr18:35689982 | G | GACTC | 10 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.978+694_978+697dup others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 35689982 | ||||||
chr18:35690076 | A | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.978+786A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690076 | |||||||
chr18:35690219 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.979-793T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690219 | |||||||
chr18:35690234 | TAACAAAG others(7): Show |
T | 1 | a0001c0001t0001g0065 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.979-773_979-760del others(14): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr18 | 35690234 | ||||||
chr18:35690283 | A | G | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.979-729A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690283 | |||||||
chr18:35690331 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.979-681C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690331 | |||||||
chr18:35690402 | T | G | 1 | a0001c0001t0004g0147 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.979-610T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690402 | |||||||
chr18:35690587 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0161 |
7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.979-425A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690587 | |||||||
chr18:35690804 | T | G | 1 | a0001c0001t0017g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.979-208T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690804 | |||||||
chr18:35690809 | T | G | 1 | a0001c0001t0002g0045 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.979-203T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 7/11 | chr18 | 35690809 | |||||||
chr18:35691328 | A | G | 1 | a0001c0001t0003g0237 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1159+136A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691328 | |||||||
chr18:35691350 | A | C | 2 | a0001c0001t0006g0158 a0001c0001t0006g0159 |
2 | HG02922.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1159+158A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691350 | |||||||
chr18:35691430 | G | A | 75 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(72): Show |
85 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1159+238G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691430 | |||||||
chr18:35691449 | T | A | 1 | a0001c0001t0004g0132 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1159+257T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691449 | |||||||
chr18:35691464 | A | T | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1159+272A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691464 | |||||||
chr18:35691683 | C | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1159+491C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35691683 | |||||||
chr18:35692058 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1160-123A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 8/11 | chr18 | 35692058 | |||||||
chr18:35692385 | A | T | 2 | a0001c0004t0001g0125 a0001c0004t0001g0126 |
2 | HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+65A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692385 | |||||||
chr18:35692432 | A | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+112A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692432 | |||||||
chr18:35692492 | T | G | 1 | a0001c0001t0001g0227 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1299+172T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692492 | |||||||
chr18:35692645 | T | C | 41 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(38): Show |
47 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(44): Show |
intron_variant | MODIFIER | c.1299+325T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692645 | |||||||
chr18:35692819 | A | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1299+499A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35692819 | |||||||
chr18:35693006 | C | T | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+686C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693006 | |||||||
chr18:35693140 | AGGAAGTT others(10): Show |
A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1299+836_1299+852d others(19): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35693140 | ||||||
chr18:35693230 | G | A | 88 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(85): Show |
99 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.1299+910G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693230 | |||||||
chr18:35693278 | G | A | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+958G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693278 | |||||||
chr18:35693293 | A | G | 32 | a0001c0001t0003g0282 a0001c0001t0004g0001 a0001c0001t0004g0122 others(29): Show |
36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1299+973A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693293 | |||||||
chr18:35693589 | T | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1299+1269T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693589 | |||||||
chr18:35693842 | T | C | 51 | a0001c0001t0001g0127 a0001c0001t0001g0262 a0001c0001t0001g0285 others(48): Show |
57 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(54): Show |
intron_variant | MODIFIER | c.1299+1522T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35693842 | |||||||
chr18:35694023 | G | A | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1299+1703G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694023 | |||||||
chr18:35694178 | T | G | 1 | a0001c0001t0001g0182 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1299+1858T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694178 | |||||||
chr18:35694220 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1299+1900A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694220 | |||||||
chr18:35694302 | A | G | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1299+1982A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694302 | |||||||
chr18:35694518 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+2198G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694518 | |||||||
chr18:35694566 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2246A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694566 | |||||||
chr18:35694601 | C | T | 1 | a0001c0001t0001g0069 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1299+2281C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694601 | |||||||
chr18:35694602 | G | T | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1299+2282G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694602 | |||||||
chr18:35694608 | T | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+2288T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694608 | |||||||
chr18:35694663 | G | A | 1 | a0001c0001t0003g0240 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1299+2343G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694663 | |||||||
chr18:35694669 | G | A | 5 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0125 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+2349G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694669 | |||||||
chr18:35694681 | G | A | 86 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(83): Show |
96 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.1299+2361G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694681 | |||||||
chr18:35694694 | C | T | 5 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0125 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1299+2374C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694694 | |||||||
chr18:35694712 | C | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1299+2392C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694712 | |||||||
chr18:35694811 | A | G | 5 | a0001c0001t0006g0156 a0001c0001t0006g0157 a0001c0001t0006g0158 others(2): Show |
5 | HG01255.hp2 HG01358.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+2491A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694811 | |||||||
chr18:35694813 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1299+2493G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694813 | |||||||
chr18:35694908 | C | T | 3 | a0001c0004t0001g0125 a0001c0004t0001g0126 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+2588C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694908 | |||||||
chr18:35694953 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1299+2633G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35694953 | |||||||
chr18:35695048 | A | G | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1299+2728A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695048 | |||||||
chr18:35695360 | G | C | 1 | a0001c0001t0004g0137 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1299+3040G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695360 | |||||||
chr18:35695526 | A | G | 2 | a0001c0001t0013g0162 a0001c0001t0013g0164 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1299+3206A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695526 | |||||||
chr18:35695824 | G | A | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1299+3504G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695824 | |||||||
chr18:35695901 | T | C | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1299+3581T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695901 | |||||||
chr18:35695946 | G | A | 26 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(23): Show |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1299+3626G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695946 | |||||||
chr18:35695969 | C | T | 72 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(69): Show |
78 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1299+3649C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695969 | |||||||
chr18:35695970 | G | A | 1 | a0001c0001t0010g0189 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1299+3650G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695970 | |||||||
chr18:35695970 | G | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1299+3650G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35695970 | |||||||
chr18:35696031 | G | A | 3 | a0001c0004t0001g0125 a0001c0004t0001g0126 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+3711G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696031 | |||||||
chr18:35696075 | G | A | 2 | a0001c0001t0007g0088 a0001c0001t0007g0107 |
2 | HG02280.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1299+3755G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696075 | |||||||
chr18:35696117 | A | G | 65 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(62): Show |
72 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1299+3797A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696117 | |||||||
chr18:35696274 | C | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1299+3954C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696274 | |||||||
chr18:35696290 | A | T | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1299+3970A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696290 | |||||||
chr18:35696384 | T | G | 1 | a0001c0001t0020g0052 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1299+4064T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696384 | |||||||
chr18:35696416 | G | A | 169 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1299+4096G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696416 | |||||||
chr18:35696435 | C | T | 1 | a0001c0001t0001g0100 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1299+4115C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696435 | |||||||
chr18:35696445 | C | T | 3 | a0001c0004t0001g0125 a0001c0004t0001g0126 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1299+4125C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696445 | |||||||
chr18:35696661 | G | T | 75 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(72): Show |
85 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(82): Show |
intron_variant | MODIFIER | c.1299+4341G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696661 | |||||||
chr18:35696843 | T | G | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1299+4523T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696843 | |||||||
chr18:35696958 | A | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1299+4638A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35696958 | |||||||
chr18:35697126 | G | C | 2 | a0001c0001t0014g0221 a0001c0001t0014g0222 |
2 | HG03195.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1299+4806G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697126 | |||||||
chr18:35697148 | A | G | 1 | a0001c0001t0013g0164 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1299+4828A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697148 | |||||||
chr18:35697229 | TGA | T | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.1299+4922_1299+492 others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35697229 | ||||||
chr18:35697229 | TGAGA | T | 3 | a0001c0001t0001g0118 a0001c0001t0013g0162 a0001c0001t0013g0164 |
3 | HG01891.hp1 HG03098.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1299+4920_1299+492 others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35697229 | ||||||
chr18:35697404 | A | G | 1 | a0001c0001t0003g0275 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1299+5084A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697404 | |||||||
chr18:35697444 | G | A | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1299+5124G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697444 | |||||||
chr18:35697677 | A | G | 1 | a0001c0001t0001g0094 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1300-5220A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697677 | |||||||
chr18:35697752 | C | T | 103 | a0001c0001t0001g0014 a0001c0001t0001g0127 a0001c0001t0001g0168 others(100): Show |
114 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(111): Show |
intron_variant | MODIFIER | c.1300-5145C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697752 | |||||||
chr18:35697812 | C | G | 1 | a0001c0001t0004g0142 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1300-5085C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697812 | |||||||
chr18:35697868 | C | T | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1300-5029C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697868 | |||||||
chr18:35697959 | C | T | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-4938C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697959 | |||||||
chr18:35697992 | C | T | 29 | a0001c0001t0003g0004 a0001c0001t0003g0192 a0001c0001t0003g0220 others(26): Show |
31 | HG00408.hp2 HG02074.hp2 HG02129.hp1 others(28): Show |
intron_variant | MODIFIER | c.1300-4905C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35697992 | |||||||
chr18:35698012 | G | A | 2 | a0001c0001t0013g0162 a0001c0001t0013g0164 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1300-4885G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698012 | |||||||
chr18:35698160 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1300-4737G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698160 | |||||||
chr18:35698205 | C | T | 1 | a0001c0001t0001g0252 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1300-4692C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698205 | |||||||
chr18:35698231 | G | A | 1 | a0001c0001t0001g0090 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1300-4666G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698231 | |||||||
chr18:35698288 | C | T | 1 | a0001c0001t0007g0089 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1300-4609C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698288 | |||||||
chr18:35698401 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-4496A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698401 | |||||||
chr18:35698549 | A | T | 1 | a0001c0001t0001g0185 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1300-4348A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698549 | |||||||
chr18:35698981 | C | G | 1 | a0001c0001t0002g0017 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1300-3916C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35698981 | |||||||
chr18:35699021 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1300-3876G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699021 | |||||||
chr18:35699035 | C | G | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1300-3862C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699035 | |||||||
chr18:35699069 | T | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1300-3828T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699069 | |||||||
chr18:35699465 | G | A | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1300-3432G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699465 | |||||||
chr18:35699607 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1300-3290T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699607 | |||||||
chr18:35699693 | T | C | 2 | a0001c0001t0013g0162 a0001c0001t0013g0164 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1300-3204T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699693 | |||||||
chr18:35699775 | A | ATTC | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1300-3120_1300-311 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35699775 | ||||||
chr18:35699829 | A | G | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-3068A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699829 | |||||||
chr18:35699917 | G | A | 11 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0181 others(8): Show |
13 | HG00140.hp1 HG00280.hp2 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1300-2980G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699917 | |||||||
chr18:35699931 | C | G | 2 | a0001c0001t0006g0156 a0001c0001t0006g0157 |
2 | HG01255.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1300-2966C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35699931 | |||||||
chr18:35699992 | CA | C | 3 | a0001c0004t0001g0125 a0001c0004t0001g0126 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1300-2902delA | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35699992 | ||||||
chr18:35700178 | G | C | 33 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(30): Show |
35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1300-2719G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700178 | |||||||
chr18:35700203 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1300-2694C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700203 | |||||||
chr18:35700257 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1300-2640C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700257 | |||||||
chr18:35700285 | C | T | 1 | a0001c0001t0001g0180 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1300-2612C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700285 | |||||||
chr18:35700622 | T | C | 1 | a0001c0001t0001g0169 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1300-2275T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700622 | |||||||
chr18:35700861 | C | T | 1 | a0001c0001t0003g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1300-2036C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700861 | |||||||
chr18:35700908 | G | C | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1300-1989G>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35700908 | |||||||
chr18:35701066 | A | G | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-1831A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701066 | |||||||
chr18:35701068 | G | A | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-1829G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701068 | |||||||
chr18:35701101 | T | C | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1300-1796T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701101 | |||||||
chr18:35701127 | A | G | 12 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1300-1770A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701127 | |||||||
chr18:35701140 | T | C | 1 | a0001c0001t0004g0146 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1300-1757T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701140 | |||||||
chr18:35701202 | A | G | 3 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0161 |
7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1300-1695A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701202 | |||||||
chr18:35701217 | G | A | 1 | a0001c0001t0001g0226 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1300-1680G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701217 | |||||||
chr18:35701264 | A | G | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-1633A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701264 | |||||||
chr18:35701279 | G | T | 6 | a0001c0001t0001g0226 a0001c0001t0001g0227 a0001c0001t0001g0228 others(3): Show |
6 | HG01884.hp1 HG02896.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-1618G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701279 | |||||||
chr18:35701338 | G | A | 5 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0125 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300-1559G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701338 | |||||||
chr18:35701500 | C | T | 169 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(166): Show |
185 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.1300-1397C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701500 | |||||||
chr18:35701551 | T | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1300-1346T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701551 | |||||||
chr18:35701791 | A | G | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-1106A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701791 | |||||||
chr18:35701827 | C | T | 3 | a0001c0001t0001g0279 a0001c0001t0001g0280 a0001c0001t0001g0281 |
3 | HG02572.hp1 HG02615.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1300-1070C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701827 | |||||||
chr18:35701872 | A | G | 87 | a0001c0001t0001g0127 a0001c0001t0001g0285 a0001c0001t0002g0002 others(84): Show |
97 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(94): Show |
intron_variant | MODIFIER | c.1300-1025A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701872 | |||||||
chr18:35701955 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1300-942A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35701955 | |||||||
chr18:35702003 | C | A | 1 | a0001c0001t0005g0063 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1300-894C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702003 | |||||||
chr18:35702036 | G | T | 31 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(28): Show |
35 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1300-861G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702036 | |||||||
chr18:35702038 | A | G | 1 | a0001c0001t0001g0270 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1300-859A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702038 | |||||||
chr18:35702092 | G | A | 5 | a0001c0001t0009g0151 a0001c0001t0009g0152 a0001c0001t0009g0153 others(2): Show |
5 | HG01069.hp1 HG01071.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1300-805G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702092 | |||||||
chr18:35702167 | C | T | 1 | a0001c0001t0001g0273 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1300-730C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702167 | |||||||
chr18:35702172 | T | A | 5 | a0001c0001t0001g0012 a0001c0001t0001g0213 a0001c0001t0001g0214 others(2): Show |
6 | HG01167.hp2 HG01169.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.1300-725T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702172 | |||||||
chr18:35702225 | C | A | 2 | a0001c0001t0002g0002 a0001c0001t0002g0161 |
6 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1300-672C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702225 | |||||||
chr18:35702457 | C | G | 16 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0029 others(13): Show |
18 | HG00408.hp1 HG00609.hp1 NA18612.hp1 others(15): Show |
intron_variant | MODIFIER | c.1300-440C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702457 | |||||||
chr18:35702655 | TG | T | 5 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0125 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1300-241delG | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | chr18 | 35702655 | |||||||
chr18:35702878 | A | ATTATTTA others(6): Show |
5 | a0001c0001t0013g0162 a0001c0001t0013g0164 a0001c0004t0001g0125 others(2): Show |
5 | HG01884.hp2 HG01891.hp1 HG02258.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.1300-18_1300-6dupT others(12): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr18 | 35702878 | ||||||
chr18:35703021 | A | C | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1398+26A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703021 | |||||||
chr18:35703036 | A | AT | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1398+43dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703036 | ||||||
chr18:35703051 | C | A | 1 | a0001c0001t0003g0244 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1398+56C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703051 | |||||||
chr18:35703052 | C | CT | 27 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(24): Show |
31 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.1398+65dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703052 | ||||||
chr18:35703149 | A | AT | 42 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(39): Show |
48 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(45): Show |
intron_variant | MODIFIER | c.1398+165dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703149 | ||||||
chr18:35703176 | A | G | 10 | a0001c0001t0001g0127 a0001c0001t0009g0151 a0001c0001t0009g0152 others(7): Show |
10 | HG01069.hp1 HG01071.hp1 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.1398+181A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703176 | |||||||
chr18:35703341 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1399-168A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | chr18 | 35703341 | |||||||
chr18:35703448 | GGCATTTA others(4): Show |
G | 1 | a0001c0001t0001g0071 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1399-58_1399-48del others(11): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr18 | 35703448 | ||||||
chr18:35704276 | C | T | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+633C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704276 | |||||||
chr18:35704277 | T | TAAA | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+634_1533+635i others(5): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704277 | |||||||
chr18:35704279 | C | T | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+636C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704279 | |||||||
chr18:35704280 | T | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+637T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704280 | |||||||
chr18:35704311 | C | CT | 17 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(14): Show |
18 | HG00609.hp2 HG00639.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.1533+684dupT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35704311 | ||||||
chr18:35704311 | CT | C | 9 | a0001c0001t0001g0205 a0001c0001t0001g0211 a0001c0001t0001g0214 others(6): Show |
9 | HG00639.hp1 HG01169.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533+684delT | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35704311 | ||||||
chr18:35704497 | A | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+854A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704497 | |||||||
chr18:35704509 | T | C | 1 | a0001c0001t0001g0266 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1533+866T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704509 | |||||||
chr18:35704554 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1533+911C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704554 | |||||||
chr18:35704555 | G | A | 45 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(42): Show |
54 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1533+912G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704555 | |||||||
chr18:35704562 | T | C | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+919T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704562 | |||||||
chr18:35704573 | G | A | 1 | a0001c0001t0002g0044 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1533+930G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704573 | |||||||
chr18:35704628 | T | A | 34 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(31): Show |
36 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.1533+985T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704628 | |||||||
chr18:35704677 | T | G | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533+1034T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704677 | |||||||
chr18:35704754 | C | T | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+1111C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704754 | |||||||
chr18:35704805 | G | A | 11 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0266 others(8): Show |
11 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1533+1162G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704805 | |||||||
chr18:35704882 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1533+1239G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704882 | |||||||
chr18:35704954 | T | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+1311T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35704954 | |||||||
chr18:35705001 | G | T | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1533+1358G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705001 | |||||||
chr18:35705079 | A | G | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1533+1436A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705079 | |||||||
chr18:35705188 | A | T | 2 | a0001c0001t0001g0087 a0001c0001t0001g0097 |
2 | HG02273.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1533+1545A>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705188 | |||||||
chr18:35705218 | C | G | 74 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(71): Show |
80 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(77): Show |
intron_variant | MODIFIER | c.1533+1575C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705218 | |||||||
chr18:35705303 | G | A | 6 | a0001c0001t0001g0003 a0001c0001t0001g0116 a0001c0001t0001g0117 others(3): Show |
9 | HG02055.hp2 HG02647.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1533+1660G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705303 | |||||||
chr18:35705427 | A | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+1784A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705427 | |||||||
chr18:35705645 | A | G | 110 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0053 others(107): Show |
117 | HG00140.hp2 HG00558.hp1 HG00621.hp2 others(114): Show |
intron_variant | MODIFIER | c.1533+2002A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705645 | |||||||
chr18:35705665 | TTAAAAA | T | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2024_1533+202 others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35705665 | ||||||
chr18:35705863 | C | T | 77 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(74): Show |
83 | HG00140.hp2 HG00558.hp1 HG00642.hp2 others(80): Show |
intron_variant | MODIFIER | c.1533+2220C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35705863 | |||||||
chr18:35706208 | T | C | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2565T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706208 | |||||||
chr18:35706232 | C | T | 1 | a0001c0001t0007g0015 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1533+2589C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706232 | |||||||
chr18:35706283 | G | A | 1 | a0001c0001t0001g0070 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1533+2640G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706283 | |||||||
chr18:35706314 | C | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2671C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706314 | |||||||
chr18:35706357 | A | G | 2 | a0001c0001t0013g0162 a0001c0001t0013g0164 |
2 | HG01891.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1533+2714A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706357 | |||||||
chr18:35706503 | AAAAAT | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2866_1533+287 others(9): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35706503 | ||||||
chr18:35706569 | G | A | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1533+2926G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706569 | |||||||
chr18:35706591 | T | C | 18 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(15): Show |
18 | HG00280.hp1 HG01074.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.1533+2948T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35706591 | |||||||
chr18:35707188 | T | A | 32 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(29): Show |
36 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(33): Show |
intron_variant | MODIFIER | c.1534-2436T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707188 | |||||||
chr18:35707215 | C | A | 12 | a0001c0001t0001g0014 a0001c0001t0001g0168 a0001c0001t0001g0169 others(9): Show |
13 | HG00609.hp2 HG00639.hp2 HG02027.hp2 others(10): Show |
intron_variant | MODIFIER | c.1534-2409C>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707215 | |||||||
chr18:35707496 | T | C | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-2128T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707496 | |||||||
chr18:35707563 | G | T | 1 | a0001c0001t0008g0080 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1534-2061G>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707563 | |||||||
chr18:35707583 | T | C | 49 | a0001c0001t0001g0127 a0001c0001t0002g0002 a0001c0001t0002g0005 others(46): Show |
55 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.1534-2041T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707583 | |||||||
chr18:35707702 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1534-1922A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707702 | |||||||
chr18:35707706 | A | C | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-1918A>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707706 | |||||||
chr18:35707764 | T | C | 3 | a0001c0001t0001g0261 a0001c0001t0001g0262 a0001c0001t0001g0263 |
3 | HG02818.hp1 HG03516.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1534-1860T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707764 | |||||||
chr18:35707805 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1534-1819G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707805 | |||||||
chr18:35707871 | C | T | 30 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(27): Show |
34 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.1534-1753C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707871 | |||||||
chr18:35707885 | G | A | 25 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(22): Show |
29 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1534-1739G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707885 | |||||||
chr18:35707982 | T | C | 1 | a0001c0001t0012g0129 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1534-1642T>C | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35707982 | |||||||
chr18:35708047 | A | G | 1 | a0001c0001t0001g0285 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1534-1577A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708047 | |||||||
chr18:35708051 | T | G | 33 | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0016 others(30): Show |
35 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.1534-1573T>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708051 | |||||||
chr18:35708074 | C | G | 1 | a0001c0001t0003g0249 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1534-1550C>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708074 | |||||||
chr18:35708076 | G | A | 1 | a0001c0001t0007g0111 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1534-1548G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708076 | |||||||
chr18:35708251 | A | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-1373A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708251 | |||||||
chr18:35708408 | GAAT | G | 39 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0006 others(36): Show |
45 | HG00280.hp1 HG00408.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1534-1210_1534-120 others(7): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35708408 | ||||||
chr18:35708704 | ACTAT | A | 4 | a0001c0003t0001g0048 a0001c0003t0001g0049 a0001c0003t0001g0050 others(1): Show |
4 | HG02055.hp1 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1534-913_1534-910d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35708704 | ||||||
chr18:35708955 | G | A | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG01168.hp1 HG01169.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.1534-669G>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35708955 | |||||||
chr18:35709048 | T | A | 1 | a0001c0001t0013g0162 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1534-576T>A | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35709048 | |||||||
chr18:35709092 | C | T | 10 | a0001c0001t0004g0001 a0001c0001t0004g0130 a0001c0001t0004g0134 others(7): Show |
14 | HG01074.hp2 HG01099.hp2 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1534-532C>T | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35709092 | |||||||
chr18:35709424 | A | G | 3 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0167 |
3 | HG02257.hp2 HG02717.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1534-200A>G | GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | chr18 | 35709424 | |||||||
chr18:35709436 | T | TTC | 17 | a0001c0001t0001g0127 a0001c0001t0002g0018 a0001c0001t0002g0027 others(14): Show |
17 | HG01069.hp1 HG01071.hp1 HG01255.hp2 others(14): Show |
intron_variant | MODIFIER | c.1534-164_1534-163d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | ||||||
chr18:35709436 | T | TTCTC | 63 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0012 others(60): Show |
67 | HG00140.hp2 HG00642.hp2 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.1534-166_1534-163d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | ||||||
chr18:35709436 | T | TTCTCTC | 6 | a0001c0001t0001g0060 a0001c0001t0001g0085 a0001c0001t0001g0285 others(3): Show |
6 | HG00558.hp1 HG02083.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1534-168_1534-163d others(8): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | ||||||
chr18:35709436 | T | TTCTCTCT others(1): Show |
3 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0161 |
7 | HG02258.hp1 HG02280.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1534-170_1534-163d others(10): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | ||||||
chr18:35709436 | TTC | T | 26 | a0001c0001t0004g0001 a0001c0001t0004g0122 a0001c0001t0004g0123 others(23): Show |
30 | HG00621.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.1534-164_1534-163d others(4): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 | ||||||
chr18:35709436 | TTCTC | T | 3 | a0001c0004t0001g0125 a0001c0004t0001g0126 a0001c0004t0001g0163 |
3 | HG01884.hp2 HG02258.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1534-166_1534-163d others(6): Show |
GALNT1 | ENSG00000141429.14 | transcript | ENST00000269195.6 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr18 | 35709436 |