Item | Value |
---|---|
geneid | 83941 |
ensemblid | ENSG00000162604.13 |
hgncid | 24142 |
symbol | TM2D1 |
name | TM2 domain containing 1 |
refseq_nuc | NM_032027.3 |
refseq_prot | NP_114416.1 |
ensembl_nuc | ENST00000606498.5 |
ensembl_prot | ENSP00000475700.1 |
mane_status | MANE Select |
chr | chr1 |
start | 61681046 |
end | 61725141 |
strand | - |
ver | v1.2 |
region | chr1:61681046-61725141 |
region5000 | chr1:61676046-61730141 |
regionname0 | TM2D1_chr1_61681046_61725141 |
regionname5000 | TM2D1_chr1_61676046_61730141 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 207 | 385 | 91 | 70 | 166 | 14 | 42 | 134 | TM2D1_chr1_61676046_61730141 | TM2D1 | MAAAW others(202): Show |
chr1 | 61676046 | 61730141 |
a0002 | 0/0 | 207 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | MAAAR others(202): Show |
chr1 | 61676046 | 61730141 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 621 | 385 | 91 | 70 | 166 | 14 | 42 | TM2D1_chr1_61676046_61730141 | TM2D1 | ATGGC others(616): Show |
chr1 | 61676046 | 61730141 | ||
a0002c0002 | 0/0 | 621 | 3 | 3 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | ATGGC others(616): Show |
chr1 | 61676046 | 61730141 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 969 | 341 | 53 | 64 | 166 | 14 | 42 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(964): Show |
chr1 | 61676046 | 61730141 |
a0001c0001t0002 | 0/0 | 969 | 23 | 20 | 3 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(964): Show |
chr1 | 61676046 | 61730141 |
a0001c0001t0003 | 0/0 | 967 | 18 | 16 | 2 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(962): Show |
chr1 | 61676046 | 61730141 |
a0001c0001t0004 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(964): Show |
chr1 | 61676046 | 61730141 |
a0001c0001t0005 | 0/0 | 969 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(964): Show |
chr1 | 61676046 | 61730141 |
a0002c0002t0001 | 0/0 | 969 | 2 | 2 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(964): Show |
chr1 | 61676046 | 61730141 |
a0002c0002t0004 | 0/0 | 969 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | GAGAA others(964): Show |
chr1 | 61676046 | 61730141 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0169 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0306 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0001g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0002g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0003g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0004g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0001c0001t0005g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0002c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
a0002c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0020 | EUR | GBR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0251 | EUR | FIN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | CHS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | CHS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0286 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0362 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0210 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0281 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0323 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01243 | hp2 | a0001 | c0001 | t0003 | g0059 | AMR | PUR | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0357 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0324 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01261 | hp1 | a0001 | c0001 | t0005 | g0271 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0353 | AMR | CLM | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0183 | EUR | IBS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0071 | EUR | IBS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0048 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0053 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0302 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02055 | hp2 | a0001 | c0001 | t0002 | g0356 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02145 | hp1 | a0001 | c0001 | t0003 | g0049 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0352 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CDX | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | CDX | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | CDX | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | CDX | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0325 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0307 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0347 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0022 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0051 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0058 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0300 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0335 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02615 | hp1 | a0002 | c0002 | t0004 | g0023 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0289 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0243 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0360 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0288 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0330 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0358 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0343 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0283 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0354 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0341 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0274 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0060 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0349 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0168 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0350 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0359 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0279 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0338 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0055 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0346 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0348 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0047 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0306 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0292 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0361 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0363 | AFR | ESN | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0045 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0050 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0326 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0181 | SAS | STU | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | STU | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0301 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0320 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0336 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0334 | SAS | STU | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0316 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0331 | SAS | BEB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0308 | SAS | STU | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | YRI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0355 | AFR | YRI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | CHB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0351 | AFR | YRI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | YRI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0364 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19030 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | LWK | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | LWK | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | LWK | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0340 | AFR | LWK | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19078 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0344 | AFR | YRI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0290 | AFR | YRI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ASW | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ASW | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | TSI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0296 | EUR | TSI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0228 | EUR | TSI | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0332 | SAS | GIH | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | GIH | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0120 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0057 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0345 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0282 | AFR | MSL | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | USA | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | USA | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | LWK | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0169 | REF | REF | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0077 | REF | REF | TM2D1_chr1_61676046_61730141 | TM2D1 | chr1 | 61676046 | 61730141 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:61725108 | A | G | 1 | a0002 | 3 | HG02280.hp2 HG02615.hp1 HG02630.hp2 |
missense_variant | MODERATE | c.13T>C | p.Trp5Arg | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/7 | 34/969 | 13/624 | 5/207 | chr1 | 61725108 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:61681112 | G | T | 2 | a0001c0001t0004 a0002c0002t0004 |
3 | HG02615.hp1 HG02818.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*258C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 7/7 | 2324 | chr1 | 61681112 | ||||||
chr1:61681115 | TAA | T | 1 | a0001c0001t0003 | 18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*253_*254delTT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 7/7 | 2319 | chr1 | 61681115 | ||||||
chr1:61681289 | A | T | 1 | a0001c0001t0005 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*81T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 7/7 | 2147 | chr1 | 61681289 | ||||||
chr1:61681347 | A | T | 1 | a0001c0001t0002 | 23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*23T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 7/7 | 2089 | chr1 | 61681347 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:61681373 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.*20-23C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61681373 | |||||||
chr1:61681477 | G | A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.*20-127C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61681477 | |||||||
chr1:61681582 | T | C | 1 | a0001c0001t0001g0320 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.*20-232A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61681582 | |||||||
chr1:61681731 | T | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0201 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*20-381A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61681731 | |||||||
chr1:61681733 | A | T | 2 | a0001c0001t0001g0179 a0001c0001t0001g0201 |
2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.*20-383T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61681733 | |||||||
chr1:61682294 | G | A | 2 | a0001c0001t0001g0112 a0001c0001t0001g0224 |
2 | NA18612.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.*20-944C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682294 | |||||||
chr1:61682379 | A | G | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
118 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(115): Show |
intron_variant | MODIFIER | c.*20-1029T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682379 | |||||||
chr1:61682518 | C | A | 1 | a0001c0001t0001g0270 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.*19+899G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682518 | |||||||
chr1:61682552 | T | A | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG00738.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.*19+865A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682552 | |||||||
chr1:61682693 | A | G | 360 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(357): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.*19+724T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682693 | |||||||
chr1:61682755 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0233 a0001c0001t0001g0236 |
4 | HG01192.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.*19+662A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682755 | |||||||
chr1:61682764 | G | A | 1 | a0001c0001t0001g0242 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.*19+653C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682764 | |||||||
chr1:61682770 | G | T | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.*19+647C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682770 | |||||||
chr1:61682841 | C | G | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.*19+576G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682841 | |||||||
chr1:61682892 | C | CA | 27 | a0001c0001t0001g0092 a0001c0001t0001g0120 a0001c0001t0001g0211 others(24): Show |
29 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(26): Show |
intron_variant | MODIFIER | c.*19+524dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682892 | |||||||
chr1:61682892 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.*19+514_*19+524del others(11): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682892 | |||||||
chr1:61682939 | A | G | 74 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
79 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.*19+478T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682939 | |||||||
chr1:61682966 | T | C | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.*19+451A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61682966 | |||||||
chr1:61683255 | G | A | 118 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(115): Show |
122 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(119): Show |
intron_variant | MODIFIER | c.*19+162C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61683255 | |||||||
chr1:61683296 | C | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.*19+121G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61683296 | |||||||
chr1:61683395 | C | CAT | 12 | a0001c0001t0001g0006 a0001c0001t0001g0119 a0001c0001t0001g0136 others(9): Show |
13 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.*19+20_*19+21dupAT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61683395 | |||||||
chr1:61683395 | C | CATAT | 10 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG00673.hp1 NA18747.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.*19+18_*19+21dupAT others(2): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 6/6 | chr1 | 61683395 | |||||||
chr1:61683565 | C | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.514-19G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61683565 | |||||||
chr1:61683682 | AT | A | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.514-137delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61683682 | |||||||
chr1:61683921 | C | CT | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-376dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61683921 | |||||||
chr1:61683934 | A | G | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.514-388T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61683934 | |||||||
chr1:61684303 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.514-757G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684303 | |||||||
chr1:61684322 | T | C | 1 | a0001c0001t0001g0209 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.514-776A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684322 | |||||||
chr1:61684369 | A | G | 360 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(357): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.514-823T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684369 | |||||||
chr1:61684557 | G | A | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-1011C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684557 | |||||||
chr1:61684598 | T | C | 13 | a0001c0001t0002g0003 a0001c0001t0002g0348 a0001c0001t0002g0349 others(10): Show |
15 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.514-1052A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684598 | |||||||
chr1:61684613 | T | C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0172 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.514-1067A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684613 | |||||||
chr1:61684649 | T | C | 2 | a0001c0001t0001g0007 a0001c0001t0001g0105 |
3 | HG02622.hp1 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.514-1103A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684649 | |||||||
chr1:61684682 | T | TAAC | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(320): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.514-1139_514-1137d others(5): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684682 | |||||||
chr1:61684699 | C | CA | 5 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0207 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-1154dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684699 | |||||||
chr1:61684759 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.514-1213T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684759 | |||||||
chr1:61684869 | C | T | 41 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0029 others(38): Show |
43 | HG00733.hp1 HG01074.hp2 HG01109.hp2 others(40): Show |
intron_variant | MODIFIER | c.514-1323G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61684869 | |||||||
chr1:61685085 | G | A | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-1539C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685085 | |||||||
chr1:61685133 | T | C | 1 | a0001c0001t0003g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.514-1587A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685133 | |||||||
chr1:61685154 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.514-1608A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685154 | |||||||
chr1:61685303 | G | A | 1 | a0001c0001t0001g0281 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.514-1757C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685303 | |||||||
chr1:61685307 | C | T | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.514-1761G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685307 | |||||||
chr1:61685446 | T | C | 1 | a0001c0001t0001g0135 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.514-1900A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685446 | |||||||
chr1:61685458 | T | G | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.514-1912A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685458 | |||||||
chr1:61685530 | C | A | 28 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0210 others(25): Show |
30 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.514-1984G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685530 | |||||||
chr1:61685541 | A | G | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.514-1995T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685541 | |||||||
chr1:61685721 | T | C | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.514-2175A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685721 | |||||||
chr1:61685825 | A | G | 1 | a0001c0001t0001g0296 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.514-2279T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685825 | |||||||
chr1:61685924 | G | C | 1 | a0001c0001t0001g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.514-2378C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61685924 | |||||||
chr1:61686029 | C | T | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.514-2483G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686029 | |||||||
chr1:61686070 | G | A | 112 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(109): Show |
115 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(112): Show |
intron_variant | MODIFIER | c.514-2524C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686070 | |||||||
chr1:61686101 | A | G | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(82): Show |
94 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.514-2555T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686101 | |||||||
chr1:61686233 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.514-2687A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686233 | |||||||
chr1:61686250 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.514-2704T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686250 | |||||||
chr1:61686311 | TA | T | 358 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(355): Show |
382 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(379): Show |
intron_variant | MODIFIER | c.514-2766delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686311 | |||||||
chr1:61686356 | C | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.514-2810G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686356 | |||||||
chr1:61686421 | C | T | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.514-2875G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686421 | |||||||
chr1:61686435 | T | C | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.514-2889A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686435 | |||||||
chr1:61686493 | C | CA | 6 | a0001c0001t0001g0080 a0001c0001t0001g0085 a0001c0001t0001g0197 others(3): Show |
6 | HG02109.hp2 HG02622.hp2 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.514-2948dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686493 | |||||||
chr1:61686643 | A | C | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(84): Show |
96 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.514-3097T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686643 | |||||||
chr1:61686710 | T | A | 1 | a0001c0001t0001g0231 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.514-3164A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686710 | |||||||
chr1:61686756 | G | A | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.514-3210C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686756 | |||||||
chr1:61686796 | T | C | 1 | a0001c0001t0001g0026 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.514-3250A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61686796 | |||||||
chr1:61687300 | T | A | 1 | a0001c0001t0003g0047 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.514-3754A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687300 | |||||||
chr1:61687340 | A | C | 1 | a0002c0002t0004g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.514-3794T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687340 | |||||||
chr1:61687517 | T | C | 2 | a0001c0001t0001g0244 a0001c0001t0001g0364 |
2 | HG00423.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.514-3971A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687517 | |||||||
chr1:61687620 | A | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.514-4074T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687620 | |||||||
chr1:61687689 | T | C | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.514-4143A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687689 | |||||||
chr1:61687706 | GA | G | 115 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(112): Show |
119 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(116): Show |
intron_variant | MODIFIER | c.514-4161delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687706 | |||||||
chr1:61687762 | G | A | 1 | a0001c0001t0001g0241 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.514-4216C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61687762 | |||||||
chr1:61688012 | T | A | 1 | a0001c0001t0001g0304 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.514-4466A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688012 | |||||||
chr1:61688044 | C | T | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.514-4498G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688044 | |||||||
chr1:61688126 | A | G | 3 | a0001c0001t0004g0282 a0001c0001t0004g0283 a0002c0002t0004g0023 |
3 | HG02615.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.514-4580T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688126 | |||||||
chr1:61688214 | G | T | 1 | a0001c0001t0001g0288 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.514-4668C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688214 | |||||||
chr1:61688315 | G | A | 1 | a0001c0001t0001g0200 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.514-4769C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688315 | |||||||
chr1:61688541 | G | C | 1 | a0002c0002t0004g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.514-4995C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688541 | |||||||
chr1:61688583 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.514-5037G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688583 | |||||||
chr1:61688742 | C | CA | 34 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0018 others(31): Show |
37 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(34): Show |
intron_variant | MODIFIER | c.514-5197dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688742 | |||||||
chr1:61688843 | GA | G | 235 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
247 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.514-5298delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688843 | |||||||
chr1:61688862 | T | C | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.514-5316A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688862 | |||||||
chr1:61688874 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.514-5328T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61688874 | |||||||
chr1:61689020 | G | A | 2 | a0001c0001t0001g0070 a0001c0001t0001g0230 |
2 | HG03491.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.514-5474C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689020 | |||||||
chr1:61689111 | A | G | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.514-5565T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689111 | |||||||
chr1:61689120 | G | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0207 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.514-5574C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689120 | |||||||
chr1:61689200 | C | T | 2 | a0001c0001t0001g0009 a0001c0001t0001g0167 |
3 | HG01069.hp2 HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.513+5497G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689200 | |||||||
chr1:61689364 | T | TTAG | 74 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(71): Show |
79 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.513+5332_513+5333i others(5): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689364 | |||||||
chr1:61689403 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+5294C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689403 | |||||||
chr1:61689408 | T | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(84): Show |
96 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.513+5289A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689408 | |||||||
chr1:61689596 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(320): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.513+5101A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689596 | |||||||
chr1:61689938 | T | A | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0098 others(1): Show |
4 | HG00735.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+4759A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689938 | |||||||
chr1:61689981 | C | A | 1 | a0001c0001t0001g0331 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.513+4716G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61689981 | |||||||
chr1:61690134 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.513+4563T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690134 | |||||||
chr1:61690324 | G | A | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
118 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.513+4373C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690324 | |||||||
chr1:61690360 | G | A | 20 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(17): Show |
20 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.513+4337C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690360 | |||||||
chr1:61690456 | C | CA | 9 | a0001c0001t0001g0034 a0001c0001t0001g0099 a0001c0001t0001g0226 others(6): Show |
9 | HG00735.hp1 HG01109.hp1 HG01981.hp2 others(6): Show |
intron_variant | MODIFIER | c.513+4240dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690456 | |||||||
chr1:61690456 | CA | C | 174 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(171): Show |
184 | HG00099.hp2 HG00438.hp2 HG00673.hp2 others(181): Show |
intron_variant | MODIFIER | c.513+4240delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690456 | |||||||
chr1:61690456 | CAA | C | 49 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0073 others(46): Show |
51 | HG00639.hp1 HG00639.hp2 HG00735.hp2 others(48): Show |
intron_variant | MODIFIER | c.513+4239_513+4240d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690456 | |||||||
chr1:61690456 | CAAA | C | 37 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0001g0020 others(34): Show |
42 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.513+4238_513+4240d others(5): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690456 | |||||||
chr1:61690456 | CAAAA | C | 21 | a0001c0001t0001g0002 a0001c0001t0001g0285 a0001c0001t0001g0324 others(18): Show |
25 | HG01070.hp1 HG01070.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.513+4237_513+4240d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690456 | |||||||
chr1:61690646 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.513+4051A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690646 | |||||||
chr1:61690662 | T | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+4035A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690662 | |||||||
chr1:61690844 | C | T | 1 | a0001c0001t0003g0044 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.513+3853G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61690844 | |||||||
chr1:61691066 | G | A | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(84): Show |
96 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.513+3631C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691066 | |||||||
chr1:61691119 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.513+3578G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691119 | |||||||
chr1:61691181 | C | T | 28 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0210 others(25): Show |
30 | HG00639.hp2 HG00735.hp2 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.513+3516G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691181 | |||||||
chr1:61691410 | G | A | 1 | a0001c0001t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.513+3287C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691410 | |||||||
chr1:61691495 | C | CA | 72 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0015 others(69): Show |
76 | HG00438.hp2 HG00639.hp2 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.513+3201dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691495 | |||||||
chr1:61691495 | C | CAA | 49 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0014 others(46): Show |
52 | HG00099.hp2 HG00733.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.513+3200_513+3201d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691495 | |||||||
chr1:61691495 | CA | C | 21 | a0001c0001t0001g0080 a0001c0001t0001g0087 a0001c0001t0001g0106 others(18): Show |
21 | HG01074.hp2 HG01109.hp2 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.513+3201delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691495 | |||||||
chr1:61691588 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.513+3109G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691588 | |||||||
chr1:61691596 | C | T | 1 | a0001c0001t0001g0328 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.513+3101G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691596 | |||||||
chr1:61691658 | A | G | 360 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(357): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.513+3039T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691658 | |||||||
chr1:61691720 | G | A | 235 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
247 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.513+2977C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691720 | |||||||
chr1:61691807 | C | G | 1 | a0001c0001t0001g0181 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.513+2890G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691807 | |||||||
chr1:61691830 | G | A | 28 | a0001c0001t0001g0011 a0001c0001t0001g0071 a0001c0001t0001g0072 others(25): Show |
29 | HG00099.hp2 HG00423.hp1 HG01106.hp1 others(26): Show |
intron_variant | MODIFIER | c.513+2867C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691830 | |||||||
chr1:61691893 | C | A | 1 | a0001c0001t0001g0068 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.513+2804G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691893 | |||||||
chr1:61691897 | G | A | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.513+2800C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691897 | |||||||
chr1:61691918 | A | C | 1 | a0001c0001t0001g0241 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.513+2779T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691918 | |||||||
chr1:61691919 | C | T | 1 | a0001c0001t0001g0241 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.513+2778G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691919 | |||||||
chr1:61691921 | T | A | 1 | a0001c0001t0001g0241 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.513+2776A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691921 | |||||||
chr1:61691921 | T | TA | 49 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(46): Show |
52 | HG00099.hp2 HG00423.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.513+2775dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691921 | |||||||
chr1:61691921 | T | TAA | 40 | a0001c0001t0001g0011 a0001c0001t0001g0017 a0001c0001t0001g0024 others(37): Show |
42 | HG00673.hp1 HG01243.hp1 HG01261.hp1 others(39): Show |
intron_variant | MODIFIER | c.513+2774_513+2775d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691921 | |||||||
chr1:61691932 | A | AAAAAAAA others(10): Show |
1 | a0001c0001t0001g0127 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(19): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0116 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(4): Show |
1 | a0001c0001t0001g0007 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(13): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0109 a0001c0001t0001g0137 a0001c0001t0001g0162 others(2): Show |
5 | HG01975.hp2 HG02027.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(12): Show |
1 | a0001c0001t0001g0227 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(21): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0279 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(27): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0216 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(11): Show |
1 | a0001c0001t0001g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(6): Show |
1 | a0001c0001t0001g0105 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(15): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(8): Show |
5 | a0001c0001t0001g0064 a0001c0001t0001g0091 a0001c0001t0001g0150 others(2): Show |
5 | NA18959.hp2 NA18972.hp2 NA19009.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(10): Show |
4 | a0001c0001t0001g0089 a0001c0001t0001g0148 a0001c0001t0001g0158 others(1): Show |
4 | HG03942.hp2 NA18953.hp2 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(19): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(12): Show |
3 | a0001c0001t0001g0063 a0001c0001t0001g0094 a0001c0001t0001g0095 |
3 | NA18957.hp2 NA19082.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(21): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(16): Show |
2 | a0001c0001t0001g0104 a0001c0001t0001g0218 |
2 | HG02698.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(25): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(18): Show |
1 | a0001c0001t0001g0103 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(27): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(7): Show |
1 | a0001c0001t0001g0152 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(9): Show |
1 | a0001c0001t0001g0212 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(18): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(11): Show |
2 | a0001c0001t0001g0086 a0001c0001t0001g0156 |
2 | NA18612.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAA others(17): Show |
1 | a0001c0001t0001g0099 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(26): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(4): Show |
1 | a0001c0001t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(13): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(6): Show |
1 | a0001c0001t0001g0139 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(15): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(8): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0068 others(6): Show |
11 | HG01168.hp2 HG01433.hp1 HG01978.hp2 others(8): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(10): Show |
8 | a0001c0001t0001g0061 a0001c0001t0001g0093 a0001c0001t0001g0136 others(5): Show |
8 | HG01109.hp2 HG01167.hp2 HG01934.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(19): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(12): Show |
4 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0121 others(1): Show |
4 | HG00738.hp1 HG01496.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(21): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(14): Show |
6 | a0001c0001t0001g0085 a0001c0001t0001g0114 a0001c0001t0001g0138 others(3): Show |
6 | HG01261.hp2 HG01517.hp1 HG02074.hp1 others(3): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(23): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAAAT others(16): Show |
3 | a0001c0001t0001g0131 a0001c0001t0001g0159 a0001c0001t0001g0228 |
3 | HG01346.hp2 NA18944.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(25): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAATA others(7): Show |
3 | a0001c0001t0001g0065 a0001c0001t0001g0069 a0001c0001t0001g0119 |
3 | HG01943.hp1 NA18974.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAATA others(9): Show |
2 | a0001c0001t0001g0092 a0001c0001t0001g0157 |
2 | HG01981.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(18): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAATA others(11): Show |
1 | a0001c0001t0001g0278 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAAATA others(13): Show |
3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0132 |
3 | HG01515.hp2 HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(22): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAATAT others(8): Show |
5 | a0001c0001t0001g0125 a0001c0001t0001g0145 a0001c0001t0001g0153 others(2): Show |
5 | HG01358.hp2 HG02132.hp1 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAATAT others(10): Show |
5 | a0001c0001t0001g0135 a0001c0001t0001g0142 a0001c0001t0001g0211 others(2): Show |
5 | NA18957.hp1 NA18978.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(19): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAATAT others(12): Show |
4 | a0001c0001t0001g0005 a0001c0001t0001g0088 a0001c0001t0001g0111 others(1): Show |
5 | HG00673.hp2 HG01069.hp1 HG01071.hp2 others(2): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(21): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAATAT others(14): Show |
3 | a0001c0001t0001g0082 a0001c0001t0001g0122 a0001c0001t0001g0154 |
3 | HG03017.hp1 HG03834.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(23): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAATAT others(16): Show |
6 | a0001c0001t0001g0079 a0001c0001t0001g0106 a0001c0001t0001g0117 others(3): Show |
6 | HG00423.hp2 HG00438.hp1 HG03710.hp2 others(3): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(25): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAAATAT others(18): Show |
2 | a0001c0001t0001g0081 a0001c0001t0001g0102 |
2 | HG02080.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(27): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAATATA others(7): Show |
2 | a0001c0001t0001g0118 a0001c0001t0001g0143 |
2 | HG00733.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAATATA others(9): Show |
2 | a0001c0001t0001g0083 a0001c0001t0001g0096 |
2 | HG02040.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(18): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAATATA others(13): Show |
1 | a0001c0001t0001g0130 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(22): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAAATATA others(17): Show |
1 | a0001c0001t0001g0087 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(26): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(6): Show |
1 | a0001c0001t0001g0100 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(15): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(8): Show |
3 | a0001c0001t0001g0101 a0001c0001t0001g0124 a0001c0001t0001g0134 |
3 | HG02165.hp2 NA18747.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(10): Show |
4 | a0001c0001t0001g0120 a0001c0001t0001g0155 a0001c0001t0001g0217 others(1): Show |
4 | HG02109.hp1 NA18964.hp2 NA19067.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2764_513+2765i others(19): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(12): Show |
3 | a0001c0001t0001g0080 a0001c0001t0001g0112 a0001c0001t0001g0270 |
3 | NA18612.hp1 NA18945.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(21): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(14): Show |
2 | a0001c0001t0001g0110 a0001c0001t0001g0123 |
2 | NA18949.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.513+2764_513+2765i others(23): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(16): Show |
1 | a0001c0001t0001g0220 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(25): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AAATATAT others(18): Show |
1 | a0001c0001t0001g0161 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(27): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | AATATATA others(11): Show |
1 | a0001c0001t0001g0108 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.513+2747_513+2764d others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | ATATATAT others(10): Show |
1 | a0001c0001t0001g0113 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.513+2764_513+2765i others(19): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | ATATATAT others(14): Show |
1 | a0001c0001t0001g0133 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.513+2764_513+2765i others(23): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | A | T | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.513+2765T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | AAT | A | 10 | a0001c0001t0001g0013 a0001c0001t0001g0018 a0001c0001t0001g0233 others(7): Show |
12 | HG01192.hp2 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.513+2763_513+2764d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691932 | AATAT | A | 24 | a0001c0001t0001g0274 a0001c0001t0001g0337 a0001c0001t0001g0339 others(21): Show |
24 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.513+2761_513+2764d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691932 | |||||||
chr1:61691933 | A | AAAAAAAT others(15): Show |
1 | a0001c0001t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.513+2763_513+2764i others(24): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691933 | |||||||
chr1:61691933 | AT | A | 42 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0016 others(39): Show |
51 | HG00099.hp1 HG00280.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.513+2763delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691933 | |||||||
chr1:61691933 | ATAT | A | 4 | a0001c0001t0001g0298 a0001c0001t0002g0344 a0001c0001t0003g0044 others(1): Show |
4 | HG02572.hp2 HG02886.hp1 NA18942.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+2761_513+2763d others(5): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691933 | |||||||
chr1:61691933 | ATATAT | A | 10 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(7): Show |
10 | HG00738.hp2 HG01192.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.513+2759_513+2763d others(7): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691933 | |||||||
chr1:61691934 | T | A | 127 | a0001c0001t0001g0004 a0001c0001t0001g0009 a0001c0001t0001g0010 others(124): Show |
135 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.513+2763A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691934 | |||||||
chr1:61691935 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0117 |
3 | HG02895.hp1 HG02897.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.513+2762T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691935 | |||||||
chr1:61691936 | T | A | 154 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(151): Show |
170 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.513+2761A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691936 | |||||||
chr1:61691936 | T | C | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.513+2761A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691936 | |||||||
chr1:61691938 | T | A | 143 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(140): Show |
151 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(148): Show |
intron_variant | MODIFIER | c.513+2759A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691938 | |||||||
chr1:61691940 | T | A | 117 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(114): Show |
123 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(120): Show |
intron_variant | MODIFIER | c.513+2757A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691940 | |||||||
chr1:61691942 | T | A | 55 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0014 others(52): Show |
58 | HG00423.hp1 HG01069.hp2 HG01175.hp2 others(55): Show |
intron_variant | MODIFIER | c.513+2755A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691942 | |||||||
chr1:61691944 | T | A | 2 | a0001c0001t0001g0203 a0001c0001t0001g0231 |
2 | HG03927.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.513+2753A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691944 | |||||||
chr1:61691953 | A | G | 1 | a0001c0001t0001g0256 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.513+2744T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691953 | |||||||
chr1:61691957 | A | G | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+2740T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691957 | |||||||
chr1:61691961 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.513+2736C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61691961 | |||||||
chr1:61692180 | A | G | 13 | a0001c0001t0002g0003 a0001c0001t0002g0348 a0001c0001t0002g0349 others(10): Show |
15 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.513+2517T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692180 | |||||||
chr1:61692363 | C | T | 4 | a0001c0001t0001g0062 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+2334G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692363 | |||||||
chr1:61692452 | T | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.513+2245A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692452 | |||||||
chr1:61692478 | GAGAA | G | 17 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(14): Show |
17 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(14): Show |
intron_variant | MODIFIER | c.513+2215_513+2218d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692478 | |||||||
chr1:61692617 | C | T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.513+2080G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692617 | |||||||
chr1:61692733 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.513+1964A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692733 | |||||||
chr1:61692877 | TCA | T | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(63): Show |
75 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.513+1818_513+1819d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61692877 | |||||||
chr1:61693248 | T | C | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0098 others(1): Show |
4 | HG00735.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.513+1449A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693248 | |||||||
chr1:61693251 | A | C | 1 | a0001c0001t0001g0090 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.513+1446T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693251 | |||||||
chr1:61693420 | T | C | 237 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(234): Show |
249 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.513+1277A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693420 | |||||||
chr1:61693428 | C | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.513+1269G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693428 | |||||||
chr1:61693694 | C | T | 4 | a0001c0001t0001g0322 a0001c0001t0001g0323 a0001c0001t0001g0324 others(1): Show |
4 | HG01168.hp1 HG01256.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.513+1003G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693694 | |||||||
chr1:61693731 | A | G | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.513+966T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693731 | |||||||
chr1:61693845 | C | G | 1 | a0001c0001t0001g0335 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.513+852G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693845 | |||||||
chr1:61693907 | T | G | 3 | a0001c0001t0002g0359 a0001c0001t0002g0360 a0001c0001t0002g0363 |
3 | HG02630.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.513+790A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693907 | |||||||
chr1:61693921 | C | A | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.513+776G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61693921 | |||||||
chr1:61694061 | T | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.513+636A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61694061 | |||||||
chr1:61694080 | G | A | 1 | a0001c0001t0001g0237 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.513+617C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61694080 | |||||||
chr1:61694113 | T | C | 20 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(17): Show |
20 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.513+584A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61694113 | |||||||
chr1:61694133 | C | T | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.513+564G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61694133 | |||||||
chr1:61694461 | G | A | 1 | a0001c0001t0002g0352 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.513+236C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61694461 | |||||||
chr1:61694549 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0126 a0001c0001t0001g0221 |
3 | HG01074.hp1 HG01168.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.513+148C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 5/6 | chr1 | 61694549 | |||||||
chr1:61694853 | T | TTA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(24): Show |
34 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.440-85_440-84dupTA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61694853 | |||||||
chr1:61694869 | C | T | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-99G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61694869 | |||||||
chr1:61694870 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.440-100T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61694870 | |||||||
chr1:61695090 | G | A | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.440-320C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695090 | |||||||
chr1:61695171 | G | T | 1 | a0001c0001t0001g0070 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.440-401C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695171 | |||||||
chr1:61695199 | C | CA | 10 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(7): Show |
10 | HG00738.hp2 HG01192.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.440-430dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695199 | |||||||
chr1:61695307 | T | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0165 |
3 | HG00438.hp2 NA18944.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.440-537A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695307 | |||||||
chr1:61695457 | T | C | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.440-687A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695457 | |||||||
chr1:61695520 | T | C | 3 | a0001c0001t0001g0073 a0001c0001t0001g0186 a0001c0001t0001g0205 |
3 | NA19012.hp2 NA19072.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.440-750A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695520 | |||||||
chr1:61695597 | A | AT | 3 | a0001c0001t0001g0013 a0001c0001t0001g0233 a0001c0001t0001g0236 |
4 | HG01192.hp2 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.440-828dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695597 | |||||||
chr1:61695748 | A | T | 8 | a0001c0001t0001g0249 a0001c0001t0001g0256 a0001c0001t0001g0257 others(5): Show |
8 | HG02040.hp2 HG02080.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-978T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695748 | |||||||
chr1:61695921 | C | T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.440-1151G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61695921 | |||||||
chr1:61696023 | G | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.440-1253C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696023 | |||||||
chr1:61696304 | C | T | 2 | a0001c0001t0001g0251 a0001c0001t0001g0254 |
2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.440-1534G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696304 | |||||||
chr1:61696311 | G | A | 1 | a0001c0001t0001g0340 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.440-1541C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696311 | |||||||
chr1:61696359 | C | T | 1 | a0001c0001t0001g0007 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.440-1589G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696359 | |||||||
chr1:61696478 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.440-1708C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696478 | |||||||
chr1:61696499 | A | G | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.440-1729T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696499 | |||||||
chr1:61696508 | CAGCCGGG others(7): Show |
C | 1 | a0002c0002t0004g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.440-1752_440-1739d others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696508 | |||||||
chr1:61696542 | CA | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(272): Show |
294 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(291): Show |
intron_variant | MODIFIER | c.440-1773delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696542 | |||||||
chr1:61696542 | CAA | C | 7 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0112 others(4): Show |
7 | HG01069.hp2 HG02622.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-1774_440-1773d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696542 | |||||||
chr1:61696966 | G | T | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
118 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.440-2196C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61696966 | |||||||
chr1:61697065 | T | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.440-2295A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697065 | |||||||
chr1:61697377 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.440-2607C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697377 | |||||||
chr1:61697557 | GACAT | G | 232 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(229): Show |
244 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(241): Show |
intron_variant | MODIFIER | c.440-2791_440-2788d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697557 | |||||||
chr1:61697580 | T | C | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG00738.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.440-2810A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697580 | |||||||
chr1:61697622 | T | A | 1 | a0001c0001t0004g0282 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.440-2852A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697622 | |||||||
chr1:61697744 | C | T | 8 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(5): Show |
8 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.440-2974G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697744 | |||||||
chr1:61697852 | T | C | 1 | a0001c0001t0001g0007 | 2 | HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.439+3082A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697852 | |||||||
chr1:61697975 | T | C | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG00738.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+2959A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61697975 | |||||||
chr1:61698043 | C | A | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(15): Show |
25 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.439+2891G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698043 | |||||||
chr1:61698102 | C | A | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0056 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+2832G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698102 | |||||||
chr1:61698125 | G | C | 1 | a0001c0001t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.439+2809C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698125 | |||||||
chr1:61698162 | G | GT | 5 | a0001c0001t0001g0062 a0001c0001t0001g0272 a0001c0001t0001g0273 others(2): Show |
5 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.439+2771dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698162 | |||||||
chr1:61698280 | C | G | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.439+2654G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698280 | |||||||
chr1:61698348 | T | C | 1 | a0001c0001t0002g0356 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.439+2586A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698348 | |||||||
chr1:61698553 | C | T | 25 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(22): Show |
25 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.439+2381G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698553 | |||||||
chr1:61698557 | T | TA | 71 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(68): Show |
80 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.439+2376dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698557 | |||||||
chr1:61698557 | T | TAA | 8 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(5): Show |
8 | HG02280.hp1 HG02486.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.439+2375_439+2376d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698557 | |||||||
chr1:61698623 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.439+2311C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698623 | |||||||
chr1:61698664 | A | G | 3 | a0001c0001t0001g0300 a0001c0001t0001g0301 a0001c0001t0001g0316 |
3 | HG02602.hp1 HG03704.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.439+2270T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698664 | |||||||
chr1:61698674 | A | G | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.439+2260T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698674 | |||||||
chr1:61698739 | AT | A | 62 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(59): Show |
71 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(68): Show |
intron_variant | MODIFIER | c.439+2194delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698739 | |||||||
chr1:61698756 | T | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0223 |
2 | HG01167.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.439+2178A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698756 | |||||||
chr1:61698841 | T | C | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.439+2093A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698841 | |||||||
chr1:61698876 | C | T | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.439+2058G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698876 | |||||||
chr1:61698944 | G | A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.439+1990C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61698944 | |||||||
chr1:61699062 | G | C | 48 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0080 others(45): Show |
49 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(46): Show |
intron_variant | MODIFIER | c.439+1872C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699062 | |||||||
chr1:61699330 | G | C | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.439+1604C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699330 | |||||||
chr1:61699346 | C | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.439+1588G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699346 | |||||||
chr1:61699464 | C | T | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(111): Show |
118 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(115): Show |
intron_variant | MODIFIER | c.439+1470G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699464 | |||||||
chr1:61699540 | A | C | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
129 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(126): Show |
intron_variant | MODIFIER | c.439+1394T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699540 | |||||||
chr1:61699541 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.439+1393T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699541 | |||||||
chr1:61699624 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.439+1310G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699624 | |||||||
chr1:61699765 | C | T | 1 | a0001c0001t0001g0212 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.439+1169G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61699765 | |||||||
chr1:61700506 | C | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0235 a0001c0001t0001g0243 |
3 | HG02109.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.439+428G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 4/6 | chr1 | 61700506 | |||||||
chr1:61701156 | C | G | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.348-131G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701156 | |||||||
chr1:61701249 | A | G | 10 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(7): Show |
10 | HG00738.hp2 HG01192.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.348-224T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701249 | |||||||
chr1:61701260 | T | C | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | NA18962.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.348-235A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701260 | |||||||
chr1:61701310 | C | CA | 25 | a0001c0001t0001g0017 a0001c0001t0001g0040 a0001c0001t0001g0062 others(22): Show |
26 | HG01069.hp2 HG01167.hp1 HG01978.hp1 others(23): Show |
intron_variant | MODIFIER | c.348-286dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | C | CAA | 91 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(88): Show |
99 | HG00099.hp2 HG00438.hp2 HG00733.hp1 others(96): Show |
intron_variant | MODIFIER | c.348-287_348-286dup others(2): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | C | CAAA | 14 | a0001c0001t0001g0031 a0001c0001t0001g0033 a0001c0001t0001g0170 others(11): Show |
14 | HG00423.hp1 HG00639.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-288_348-286dup others(3): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CA | C | 54 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0020 others(51): Show |
60 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.348-286delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CAA | C | 109 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
114 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(111): Show |
intron_variant | MODIFIER | c.348-287_348-286del others(2): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CAAA | C | 13 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0102 others(10): Show |
13 | HG01074.hp1 HG02027.hp1 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.348-288_348-286del others(3): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0276 a0001c0001t0001g0277 a0001c0001t0001g0278 others(3): Show |
6 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-294_348-286del others(9): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0275 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.348-295_348-286del others(10): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0318 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.348-296_348-286del others(11): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701310 | CAAAAAAA others(8): Show |
C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.348-300_348-286del others(15): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701310 | |||||||
chr1:61701364 | G | A | 4 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(1): Show |
4 | HG02280.hp1 HG02486.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.348-339C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701364 | |||||||
chr1:61701365 | G | A | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.348-340C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701365 | |||||||
chr1:61701366 | A | C | 1 | a0001c0001t0001g0005 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.348-341T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701366 | |||||||
chr1:61701436 | G | C | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
118 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.348-411C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701436 | |||||||
chr1:61701556 | C | CGT | 6 | a0001c0001t0001g0038 a0001c0001t0001g0273 a0001c0001t0002g0350 others(3): Show |
6 | HG01891.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.348-533_348-532dup others(2): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGT | 15 | a0001c0001t0001g0250 a0001c0001t0002g0345 a0001c0001t0002g0346 others(12): Show |
15 | HG01884.hp1 HG02280.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.348-535_348-532dup others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGTGT | 12 | a0001c0001t0001g0272 a0001c0001t0001g0274 a0001c0001t0001g0292 others(9): Show |
14 | HG01070.hp1 HG01496.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.348-537_348-532dup others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGTGTG others(1): Show |
12 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0275 others(9): Show |
12 | HG01109.hp2 HG01192.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.348-539_348-532dup others(8): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGTGTG others(3): Show |
2 | a0001c0001t0001g0286 a0001c0001t0005g0271 |
2 | HG00738.hp2 HG01261.hp1 |
intron_variant | MODIFIER | c.348-541_348-532dup others(10): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGTGTG others(5): Show |
14 | a0001c0001t0001g0277 a0001c0001t0001g0278 a0001c0001t0001g0279 others(11): Show |
14 | HG01074.hp2 HG02615.hp2 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.348-543_348-532dup others(12): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGTGTG others(7): Show |
1 | a0001c0001t0002g0360 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.348-545_348-532dup others(14): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | C | CGTGTGTG others(9): Show |
1 | a0001c0001t0001g0276 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.348-547_348-532dup others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | CGT | C | 228 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(225): Show |
247 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(244): Show |
intron_variant | MODIFIER | c.348-533_348-532del others(2): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701556 | CGTGT | C | 9 | a0001c0001t0001g0127 a0001c0001t0001g0155 a0001c0001t0001g0197 others(6): Show |
9 | HG01167.hp1 HG02109.hp2 HG02155.hp2 others(6): Show |
intron_variant | MODIFIER | c.348-535_348-532del others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701556 | |||||||
chr1:61701790 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.348-765A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701790 | |||||||
chr1:61701956 | C | T | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.348-931G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701956 | |||||||
chr1:61701987 | C | T | 17 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0081 others(14): Show |
17 | HG00438.hp1 HG00673.hp2 HG02056.hp2 others(14): Show |
intron_variant | MODIFIER | c.348-962G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61701987 | |||||||
chr1:61702206 | A | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348-1181T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702206 | |||||||
chr1:61702269 | C | T | 8 | a0001c0001t0001g0249 a0001c0001t0001g0256 a0001c0001t0001g0257 others(5): Show |
8 | HG02040.hp2 HG02080.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-1244G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702269 | |||||||
chr1:61702289 | A | T | 1 | a0001c0001t0002g0346 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.348-1264T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702289 | |||||||
chr1:61702376 | C | CT | 19 | a0001c0001t0001g0126 a0001c0001t0003g0043 a0001c0001t0003g0044 others(16): Show |
19 | HG00639.hp1 HG01168.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.348-1352dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702376 | |||||||
chr1:61702420 | G | A | 3 | a0001c0001t0004g0282 a0001c0001t0004g0283 a0002c0002t0004g0023 |
3 | HG02615.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.348-1395C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702420 | |||||||
chr1:61702523 | C | G | 1 | a0001c0001t0001g0285 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.348-1498G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702523 | |||||||
chr1:61702566 | C | G | 1 | a0001c0001t0001g0225 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.348-1541G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702566 | |||||||
chr1:61702611 | A | T | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.348-1586T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702611 | |||||||
chr1:61702628 | A | G | 1 | a0001c0001t0003g0056 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.348-1603T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702628 | |||||||
chr1:61702671 | T | C | 1 | a0001c0001t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.348-1646A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702671 | |||||||
chr1:61702750 | T | TTA | 4 | a0001c0001t0001g0027 a0001c0001t0001g0278 a0002c0002t0001g0021 others(1): Show |
4 | HG01074.hp2 HG02280.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-1727_348-1726d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702750 | |||||||
chr1:61702936 | C | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.348-1911G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702936 | |||||||
chr1:61702962 | C | T | 9 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(6): Show |
16 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(13): Show |
intron_variant | MODIFIER | c.348-1937G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61702962 | |||||||
chr1:61703020 | C | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.348-1995G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703020 | |||||||
chr1:61703045 | G | T | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.348-2020C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703045 | |||||||
chr1:61703049 | T | G | 1 | a0001c0001t0001g0246 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.348-2024A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703049 | |||||||
chr1:61703081 | G | C | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.348-2056C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703081 | |||||||
chr1:61703226 | A | G | 3 | a0001c0001t0001g0326 a0001c0001t0001g0331 a0001c0001t0001g0334 |
3 | HG03669.hp2 HG04115.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.348-2201T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703226 | |||||||
chr1:61703251 | T | C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.348-2226A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703251 | |||||||
chr1:61703258 | T | C | 1 | a0001c0001t0001g0187 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.348-2233A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703258 | |||||||
chr1:61703282 | TATG | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.348-2260_348-2258d others(5): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703282 | |||||||
chr1:61703311 | ATAT | A | 9 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(6): Show |
9 | HG01074.hp2 HG01109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.348-2289_348-2287d others(5): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703311 | |||||||
chr1:61703413 | AT | A | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
128 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.348-2389delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703413 | |||||||
chr1:61703506 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.348-2481C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703506 | |||||||
chr1:61703628 | G | T | 4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0098 others(1): Show |
4 | HG00735.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.348-2603C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703628 | |||||||
chr1:61703718 | T | TTA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0078 others(8): Show |
11 | HG01109.hp1 HG02451.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.348-2695_348-2694d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTA | T | 22 | a0001c0001t0001g0006 a0001c0001t0001g0009 a0001c0001t0001g0010 others(19): Show |
25 | HG00438.hp2 HG00738.hp2 HG01099.hp1 others(22): Show |
intron_variant | MODIFIER | c.348-2695_348-2694d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATA | T | 45 | a0001c0001t0001g0013 a0001c0001t0001g0016 a0001c0001t0001g0018 others(42): Show |
46 | HG00639.hp2 HG00673.hp1 HG00735.hp2 others(43): Show |
intron_variant | MODIFIER | c.348-2697_348-2694d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATA | T | 76 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0008 others(73): Show |
82 | HG00099.hp2 HG00280.hp1 HG01069.hp1 others(79): Show |
intron_variant | MODIFIER | c.348-2699_348-2694d others(8): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATAT others(1): Show |
T | 122 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0012 others(119): Show |
126 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.348-2701_348-2694d others(10): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATAT others(3): Show |
T | 19 | a0001c0001t0001g0027 a0001c0001t0001g0079 a0001c0001t0001g0080 others(16): Show |
19 | HG00673.hp2 HG02080.hp2 HG02293.hp2 others(16): Show |
intron_variant | MODIFIER | c.348-2703_348-2694d others(12): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATAT others(5): Show |
T | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
20 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(17): Show |
intron_variant | MODIFIER | c.348-2705_348-2694d others(14): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATAT others(7): Show |
T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(20): Show |
27 | HG00099.hp1 HG00280.hp2 HG01074.hp2 others(24): Show |
intron_variant | MODIFIER | c.348-2707_348-2694d others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATAT others(9): Show |
T | 3 | a0001c0001t0001g0275 a0001c0001t0003g0055 a0001c0001t0003g0057 |
3 | HG02486.hp1 HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.348-2709_348-2694d others(18): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703718 | TTATATAT others(11): Show |
T | 6 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0056 others(3): Show |
6 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.348-2711_348-2694d others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703718 | |||||||
chr1:61703728 | ATATATAT others(25): Show |
A | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.348-2735_348-2704d others(34): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703728 | |||||||
chr1:61703734 | A | T | 1 | a0001c0001t0001g0305 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.348-2709T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703734 | |||||||
chr1:61703740 | A | G | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348-2715T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703740 | |||||||
chr1:61703741 | T | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348-2716A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703741 | |||||||
chr1:61703743 | TATATATA others(8): Show |
T | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348-2733_348-2719d others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703743 | |||||||
chr1:61703746 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.348-2721T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703746 | |||||||
chr1:61703747 | T | C | 2 | a0001c0001t0001g0066 a0001c0001t0001g0067 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.348-2722A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703747 | |||||||
chr1:61703748 | A | G | 1 | a0001c0001t0001g0011 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.348-2723T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703748 | |||||||
chr1:61703749 | T | C | 1 | a0001c0001t0001g0011 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.348-2724A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703749 | |||||||
chr1:61703750 | A | G | 1 | a0001c0001t0001g0255 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.348-2725T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703750 | |||||||
chr1:61703751 | T | C | 1 | a0001c0001t0001g0255 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.348-2726A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703751 | |||||||
chr1:61703752 | A | G | 2 | a0001c0001t0001g0299 a0001c0001t0001g0316 |
2 | HG04184.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.348-2727T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703752 | |||||||
chr1:61703753 | T | C | 2 | a0001c0001t0001g0299 a0001c0001t0001g0316 |
2 | HG04184.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.348-2728A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703753 | |||||||
chr1:61703756 | G | A | 1 | a0001c0001t0001g0285 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.348-2731C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703756 | |||||||
chr1:61703757 | C | T | 1 | a0001c0001t0001g0285 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.348-2732G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703757 | |||||||
chr1:61703758 | AT | A | 79 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0018 others(76): Show |
87 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.348-2734delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703758 | |||||||
chr1:61703762 | T | G | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0056 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.348-2737A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703762 | |||||||
chr1:61703771 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.348-2746A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703771 | |||||||
chr1:61703787 | G | A | 3 | a0001c0001t0003g0050 a0001c0001t0004g0282 a0002c0002t0004g0023 |
3 | HG02615.hp1 HG03471.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.348-2762C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703787 | |||||||
chr1:61703917 | C | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(18): Show |
28 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.348-2892G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703917 | |||||||
chr1:61703976 | G | A | 3 | a0001c0001t0001g0182 a0002c0002t0001g0021 a0002c0002t0001g0022 |
3 | HG02165.hp1 HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.348-2951C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61703976 | |||||||
chr1:61704052 | A | G | 302 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(299): Show |
316 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(313): Show |
intron_variant | MODIFIER | c.348-3027T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704052 | |||||||
chr1:61704148 | C | CTCAAGTG others(6): Show |
1 | a0001c0001t0001g0040 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.348-3136_348-3124d others(15): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704148 | |||||||
chr1:61704181 | C | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.348-3156G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704181 | |||||||
chr1:61704238 | C | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0122 |
2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.348-3213G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704238 | |||||||
chr1:61704242 | C | A | 2 | a0001c0001t0001g0082 a0001c0001t0001g0122 |
2 | HG03017.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.348-3217G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704242 | |||||||
chr1:61704558 | C | A | 1 | a0001c0001t0001g0098 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.348-3533G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704558 | |||||||
chr1:61704879 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.348-3854C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704879 | |||||||
chr1:61704943 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.348-3918C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61704943 | |||||||
chr1:61705142 | A | C | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.348-4117T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705142 | |||||||
chr1:61705150 | A | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.348-4125T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705150 | |||||||
chr1:61705212 | T | C | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
125 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.347+4117A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705212 | |||||||
chr1:61705279 | C | T | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.347+4050G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705279 | |||||||
chr1:61705320 | G | A | 3 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0042 |
3 | HG00673.hp1 NA18747.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.347+4009C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705320 | |||||||
chr1:61705343 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.347+3986C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705343 | |||||||
chr1:61705347 | A | G | 2 | a0001c0001t0001g0094 a0001c0001t0001g0095 |
2 | NA18957.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.347+3982T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705347 | |||||||
chr1:61705373 | A | G | 3 | a0001c0001t0001g0197 a0001c0001t0001g0235 a0001c0001t0001g0243 |
3 | HG02109.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.347+3956T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705373 | |||||||
chr1:61705702 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.347+3627C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705702 | |||||||
chr1:61705802 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.347+3527C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705802 | |||||||
chr1:61705956 | G | C | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3373C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705956 | |||||||
chr1:61705957 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3372A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705957 | |||||||
chr1:61705959 | T | A | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3370A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705959 | |||||||
chr1:61705962 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3367T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705962 | |||||||
chr1:61705963 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3366T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705963 | |||||||
chr1:61705965 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3364T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705965 | |||||||
chr1:61705966 | C | G | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3363G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705966 | |||||||
chr1:61705967 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3362T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705967 | |||||||
chr1:61705968 | A | T | 1 | a0001c0001t0001g0153 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.347+3361T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61705968 | |||||||
chr1:61706037 | C | T | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+3292G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706037 | |||||||
chr1:61706065 | A | C | 1 | a0001c0001t0001g0256 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.347+3264T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706065 | |||||||
chr1:61706351 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.347+2978C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706351 | |||||||
chr1:61706536 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
41 | HG00280.hp1 HG00673.hp1 HG01099.hp1 others(38): Show |
intron_variant | MODIFIER | c.347+2793G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706536 | |||||||
chr1:61706567 | G | A | 1 | a0001c0001t0004g0282 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.347+2762C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706567 | |||||||
chr1:61706635 | C | CA | 13 | a0001c0001t0002g0003 a0001c0001t0002g0348 a0001c0001t0002g0349 others(10): Show |
15 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+2693_347+2694i others(3): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706635 | |||||||
chr1:61706636 | C | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0348 a0001c0001t0002g0349 others(10): Show |
15 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+2693G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706636 | |||||||
chr1:61706730 | C | T | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.347+2599G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706730 | |||||||
chr1:61706751 | G | A | 235 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(232): Show |
247 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(244): Show |
intron_variant | MODIFIER | c.347+2578C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706751 | |||||||
chr1:61706765 | G | C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.347+2564C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706765 | |||||||
chr1:61706783 | C | G | 1 | a0001c0001t0001g0083 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.347+2546G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706783 | |||||||
chr1:61706834 | A | AAAAG | 38 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(35): Show |
41 | HG00438.hp2 HG01099.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.347+2491_347+2494d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(1): Show |
18 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0042 others(15): Show |
18 | HG00280.hp1 HG00673.hp1 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.347+2487_347+2494d others(10): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(5): Show |
4 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0087 others(1): Show |
4 | HG02622.hp1 HG02895.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+2483_347+2494d others(14): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(9): Show |
30 | a0001c0001t0001g0006 a0001c0001t0001g0079 a0001c0001t0001g0080 others(27): Show |
31 | HG00438.hp1 HG00735.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.347+2479_347+2494d others(18): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(13): Show |
29 | a0001c0001t0001g0015 a0001c0001t0001g0063 a0001c0001t0001g0065 others(26): Show |
29 | HG00733.hp2 HG01074.hp1 HG01081.hp1 others(26): Show |
intron_variant | MODIFIER | c.347+2475_347+2494d others(22): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(17): Show |
22 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0015 others(19): Show |
24 | HG00673.hp2 HG01069.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.347+2471_347+2494d others(26): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(21): Show |
10 | a0001c0001t0001g0008 a0001c0001t0001g0061 a0001c0001t0001g0069 others(7): Show |
11 | HG01099.hp2 HG01346.hp2 HG01934.hp2 others(8): Show |
intron_variant | MODIFIER | c.347+2467_347+2494d others(30): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(25): Show |
12 | a0001c0001t0001g0083 a0001c0001t0001g0112 a0001c0001t0001g0114 others(9): Show |
12 | HG00423.hp2 HG00738.hp1 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.347+2494_347+2495i others(34): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(29): Show |
2 | a0001c0001t0001g0138 a0001c0001t0001g0146 |
2 | HG01261.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.347+2494_347+2495i others(38): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAAGAAA others(33): Show |
1 | a0001c0001t0001g0120 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.347+2494_347+2495i others(42): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAAGAAAG others(24): Show |
1 | a0001c0001t0001g0092 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.347+2494_347+2495i others(33): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAGAAAGA others(15): Show |
1 | a0001c0001t0001g0093 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.347+2494_347+2495i others(24): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | A | AAGAAGAA others(22): Show |
1 | a0001c0001t0001g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.347+2494_347+2495i others(31): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | AAAAG | A | 68 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(65): Show |
77 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(74): Show |
intron_variant | MODIFIER | c.347+2491_347+2494d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | AAAAGAAA others(1): Show |
A | 19 | a0001c0001t0001g0247 a0001c0001t0001g0317 a0001c0001t0003g0044 others(16): Show |
19 | HG00639.hp1 HG00639.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.347+2487_347+2494d others(10): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706834 | AAAAGAAA others(5): Show |
A | 3 | a0001c0001t0004g0282 a0001c0001t0004g0283 a0002c0002t0004g0023 |
3 | HG02615.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.347+2483_347+2494d others(14): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706834 | |||||||
chr1:61706951 | A | G | 3 | a0001c0001t0002g0359 a0001c0001t0002g0360 a0001c0001t0002g0363 |
3 | HG02630.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.347+2378T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706951 | |||||||
chr1:61706958 | T | C | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+2371A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61706958 | |||||||
chr1:61707131 | T | C | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+2198A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707131 | |||||||
chr1:61707179 | A | T | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.347+2150T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707179 | |||||||
chr1:61707215 | G | A | 10 | a0001c0001t0001g0079 a0001c0001t0001g0080 a0001c0001t0001g0100 others(7): Show |
10 | HG02165.hp2 HG02523.hp2 NA18747.hp1 others(7): Show |
intron_variant | MODIFIER | c.347+2114C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707215 | |||||||
chr1:61707277 | C | A | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.347+2052G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707277 | |||||||
chr1:61707445 | C | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.347+1884G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707445 | |||||||
chr1:61707599 | C | A | 2 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
2 | HG01243.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.347+1730G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707599 | |||||||
chr1:61707608 | T | C | 2 | a0001c0001t0001g0322 a0001c0001t0001g0323 |
2 | HG01168.hp1 HG01256.hp2 |
intron_variant | MODIFIER | c.347+1721A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707608 | |||||||
chr1:61707759 | C | T | 1 | a0001c0001t0003g0043 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.347+1570G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707759 | |||||||
chr1:61707763 | A | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0025 others(9): Show |
14 | HG00438.hp2 HG01069.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.347+1566T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707763 | |||||||
chr1:61707868 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+1461G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707868 | |||||||
chr1:61707898 | C | A | 8 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(5): Show |
8 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.347+1431G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61707898 | |||||||
chr1:61708087 | G | A | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.347+1242C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708087 | |||||||
chr1:61708147 | C | G | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.347+1182G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708147 | |||||||
chr1:61708278 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.347+1051C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708278 | |||||||
chr1:61708484 | G | A | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0056 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.347+845C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708484 | |||||||
chr1:61708687 | T | C | 1 | a0001c0001t0001g0296 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.347+642A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708687 | |||||||
chr1:61708857 | T | TA | 11 | a0001c0001t0001g0197 a0001c0001t0001g0235 a0001c0001t0001g0243 others(8): Show |
11 | HG02109.hp2 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.347+471dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708857 | |||||||
chr1:61708857 | TA | T | 8 | a0001c0001t0001g0029 a0001c0001t0001g0073 a0001c0001t0001g0087 others(5): Show |
8 | HG02922.hp1 NA18962.hp1 NA18978.hp1 others(5): Show |
intron_variant | MODIFIER | c.347+471delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708857 | |||||||
chr1:61708859 | A | T | 3 | a0001c0001t0002g0359 a0001c0001t0002g0360 a0001c0001t0002g0363 |
3 | HG02630.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.347+470T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708859 | |||||||
chr1:61708946 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.347+383A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708946 | |||||||
chr1:61708963 | G | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.347+366C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708963 | |||||||
chr1:61708968 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.347+361G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708968 | |||||||
chr1:61708979 | A | G | 1 | a0001c0001t0003g0051 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.347+350T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708979 | |||||||
chr1:61708983 | T | G | 1 | a0001c0001t0001g0323 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.347+346A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61708983 | |||||||
chr1:61709056 | T | G | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
121 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.347+273A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61709056 | |||||||
chr1:61709291 | AAGTAATC others(8): Show |
A | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.347+23_347+37delAA others(13): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61709291 | |||||||
chr1:61709299 | T | C | 28 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(25): Show |
30 | HG01070.hp1 HG01074.hp2 HG01109.hp2 others(27): Show |
intron_variant | MODIFIER | c.347+30A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 3/6 | chr1 | 61709299 | |||||||
chr1:61709588 | C | A | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.239-151G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61709588 | |||||||
chr1:61709648 | A | G | 1 | a0001c0001t0001g0238 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.239-211T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61709648 | |||||||
chr1:61709668 | C | T | 85 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(82): Show |
94 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(91): Show |
intron_variant | MODIFIER | c.239-231G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61709668 | |||||||
chr1:61709791 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.239-354A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61709791 | |||||||
chr1:61709868 | C | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(64): Show |
76 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.239-431G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61709868 | |||||||
chr1:61710055 | T | C | 1 | a0001c0001t0001g0170 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.239-618A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710055 | |||||||
chr1:61710099 | T | G | 114 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(111): Show |
118 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(115): Show |
intron_variant | MODIFIER | c.239-662A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710099 | |||||||
chr1:61710103 | T | C | 2 | a0001c0001t0001g0184 a0001c0001t0001g0237 |
2 | NA18994.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.239-666A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710103 | |||||||
chr1:61710206 | C | A | 1 | a0001c0001t0003g0059 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.239-769G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710206 | |||||||
chr1:61710269 | T | C | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(64): Show |
76 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.239-832A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710269 | |||||||
chr1:61710280 | G | T | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-843C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710280 | |||||||
chr1:61710337 | G | A | 1 | a0001c0001t0003g0053 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.239-900C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710337 | |||||||
chr1:61710425 | C | CA | 32 | a0001c0001t0001g0018 a0001c0001t0001g0039 a0001c0001t0001g0070 others(29): Show |
33 | HG00735.hp2 HG01074.hp2 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.239-989dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710425 | |||||||
chr1:61710425 | CA | C | 16 | a0001c0001t0001g0062 a0001c0001t0001g0272 a0001c0001t0001g0273 others(13): Show |
16 | HG01884.hp1 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.239-989delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710425 | |||||||
chr1:61710425 | CAA | C | 6 | a0001c0001t0003g0053 a0001c0001t0003g0056 a0001c0001t0003g0057 others(3): Show |
6 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-990_239-989del others(2): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710425 | |||||||
chr1:61710445 | AAT | A | 11 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(8): Show |
11 | NA18612.hp2 NA18943.hp2 NA18944.hp2 others(8): Show |
intron_variant | MODIFIER | c.239-1010_239-1009d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710445 | |||||||
chr1:61710446 | A | AG | 2 | a0001c0001t0001g0007 a0001c0001t0001g0124 |
3 | HG02165.hp2 HG03139.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.239-1010_239-1009i others(3): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710446 | |||||||
chr1:61710446 | A | G | 1 | a0001c0001t0002g0362 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.239-1009T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710446 | |||||||
chr1:61710446 | AT | A | 97 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(94): Show |
102 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(99): Show |
intron_variant | MODIFIER | c.239-1010delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710446 | |||||||
chr1:61710447 | T | A | 13 | a0001c0001t0001g0069 a0001c0001t0001g0080 a0001c0001t0001g0086 others(10): Show |
13 | HG00423.hp2 HG00738.hp1 HG01081.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-1010A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710447 | |||||||
chr1:61710448 | G | A | 5 | a0001c0001t0001g0007 a0001c0001t0001g0124 a0001c0001t0001g0286 others(2): Show |
6 | HG00738.hp2 HG01070.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-1011C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710448 | |||||||
chr1:61710448 | G | GTA | 16 | a0001c0001t0001g0016 a0001c0001t0001g0247 a0001c0001t0001g0248 others(13): Show |
19 | HG01099.hp1 HG01109.hp1 HG01433.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-1013_239-1012d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710448 | |||||||
chr1:61710448 | G | GTATA | 5 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0001c0001t0002g0356 others(2): Show |
5 | HG01255.hp2 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-1015_239-1012d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710448 | |||||||
chr1:61710461 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.239-1024A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710461 | |||||||
chr1:61710463 | C | T | 5 | a0001c0001t0001g0071 a0001c0001t0001g0172 a0001c0001t0002g0350 others(2): Show |
5 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-1026G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710463 | |||||||
chr1:61710463 | CAT | C | 14 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(11): Show |
14 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(11): Show |
intron_variant | MODIFIER | c.239-1028_239-1027d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710463 | |||||||
chr1:61710465 | T | C | 5 | a0001c0001t0001g0071 a0001c0001t0001g0172 a0001c0001t0002g0350 others(2): Show |
5 | HG01496.hp2 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-1028A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710465 | |||||||
chr1:61710473 | T | TAC | 6 | a0001c0001t0001g0197 a0001c0001t0001g0235 a0001c0001t0001g0243 others(3): Show |
6 | HG01168.hp1 HG01256.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-1037_239-1036i others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710473 | |||||||
chr1:61710475 | T | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0073 others(46): Show |
53 | HG00733.hp1 HG01070.hp1 HG01168.hp1 others(50): Show |
intron_variant | MODIFIER | c.239-1038A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710475 | |||||||
chr1:61710475 | T | TAC | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(64): Show |
78 | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(75): Show |
intron_variant | MODIFIER | c.239-1040_239-1039d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710475 | |||||||
chr1:61710475 | T | TACAC | 6 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0125 others(3): Show |
6 | HG02451.hp2 HG02523.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-1042_239-1039d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710475 | |||||||
chr1:61710475 | T | TACACAC | 4 | a0001c0001t0001g0062 a0001c0001t0001g0272 a0001c0001t0001g0273 others(1): Show |
4 | HG01884.hp2 HG02922.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-1044_239-1039d others(8): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710475 | |||||||
chr1:61710477 | C | T | 3 | a0001c0001t0001g0071 a0001c0001t0001g0172 a0001c0001t0003g0055 |
3 | HG01516.hp2 HG01517.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.239-1040G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710477 | |||||||
chr1:61710481 | CACACACA others(7): Show |
C | 16 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0073 others(13): Show |
18 | HG00733.hp1 HG01975.hp1 NA18943.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-1058_239-1045d others(16): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710481 | |||||||
chr1:61710483 | CACACACA others(5): Show |
C | 39 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0030 others(36): Show |
40 | HG00099.hp2 HG00423.hp1 HG01106.hp1 others(37): Show |
intron_variant | MODIFIER | c.239-1058_239-1047d others(14): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710483 | |||||||
chr1:61710485 | CACACACA others(3): Show |
C | 2 | a0001c0001t0001g0071 a0001c0001t0001g0172 |
2 | HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.239-1058_239-1049d others(12): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710485 | |||||||
chr1:61710493 | T | C | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
151 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(148): Show |
intron_variant | MODIFIER | c.239-1056A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710493 | |||||||
chr1:61710495 | T | C | 1 | a0002c0002t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-1058A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710495 | |||||||
chr1:61710497 | C | T | 146 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(143): Show |
151 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(148): Show |
intron_variant | MODIFIER | c.239-1060G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710497 | |||||||
chr1:61710499 | C | T | 1 | a0002c0002t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.239-1062G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710499 | |||||||
chr1:61710499 | CACAT | C | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-1066_239-1063d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710499 | |||||||
chr1:61710501 | C | T | 1 | a0001c0001t0002g0353 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.239-1064G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710501 | |||||||
chr1:61710503 | T | C | 136 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(133): Show |
141 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(138): Show |
intron_variant | MODIFIER | c.239-1066A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710503 | |||||||
chr1:61710503 | T | TAC | 6 | a0001c0001t0001g0027 a0001c0001t0001g0213 a0001c0001t0001g0214 others(3): Show |
6 | HG00280.hp1 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.239-1068_239-1067d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710503 | |||||||
chr1:61710503 | TAC | T | 24 | a0001c0001t0001g0125 a0001c0001t0001g0292 a0001c0001t0001g0337 others(21): Show |
24 | HG01070.hp1 HG01255.hp2 HG01261.hp1 others(21): Show |
intron_variant | MODIFIER | c.239-1068_239-1067d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710503 | |||||||
chr1:61710503 | TACAC | T | 13 | a0001c0001t0001g0339 a0001c0001t0002g0003 a0001c0001t0002g0345 others(10): Show |
13 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.239-1070_239-1067d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710503 | |||||||
chr1:61710503 | TACACACA others(5): Show |
T | 1 | a0001c0001t0003g0058 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.239-1078_239-1067d others(14): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710503 | |||||||
chr1:61710505 | C | T | 134 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(131): Show |
139 | HG00438.hp1 HG00673.hp2 HG00733.hp2 others(136): Show |
intron_variant | MODIFIER | c.239-1068G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710505 | |||||||
chr1:61710507 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.239-1070G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710507 | |||||||
chr1:61710509 | C | T | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.239-1072G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710509 | |||||||
chr1:61710511 | C | T | 1 | a0001c0001t0002g0353 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.239-1074G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710511 | |||||||
chr1:61710638 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.239-1201C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710638 | |||||||
chr1:61710723 | T | G | 1 | a0001c0001t0001g0089 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.239-1286A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710723 | |||||||
chr1:61710845 | T | C | 5 | a0001c0001t0001g0024 a0001c0001t0001g0075 a0001c0001t0001g0207 others(2): Show |
5 | HG01167.hp1 HG02451.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.239-1408A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710845 | |||||||
chr1:61710859 | G | A | 10 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG01074.hp2 HG01109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-1422C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710859 | |||||||
chr1:61710883 | C | G | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.239-1446G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61710883 | |||||||
chr1:61711047 | C | T | 1 | a0001c0001t0001g0091 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.239-1610G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711047 | |||||||
chr1:61711058 | G | A | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.239-1621C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711058 | |||||||
chr1:61711109 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(319): Show |
343 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(340): Show |
intron_variant | MODIFIER | c.239-1672T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711109 | |||||||
chr1:61711198 | C | T | 1 | a0001c0001t0001g0062 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.239-1761G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711198 | |||||||
chr1:61711352 | A | T | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.239-1915T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711352 | |||||||
chr1:61711355 | A | G | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(84): Show |
96 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.239-1918T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711355 | |||||||
chr1:61711408 | G | T | 1 | a0001c0001t0001g0040 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.239-1971C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711408 | |||||||
chr1:61711494 | T | A | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.239-2057A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711494 | |||||||
chr1:61711510 | G | A | 1 | a0001c0001t0001g0364 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.239-2073C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711510 | |||||||
chr1:61711625 | C | CA | 52 | a0001c0001t0001g0027 a0001c0001t0001g0086 a0001c0001t0001g0090 others(49): Show |
54 | HG00639.hp1 HG00738.hp2 HG01070.hp1 others(51): Show |
intron_variant | MODIFIER | c.239-2189dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711625 | |||||||
chr1:61711625 | C | CAA | 16 | a0001c0001t0001g0062 a0001c0001t0002g0354 a0001c0001t0002g0355 others(13): Show |
16 | HG01255.hp2 HG01884.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-2190_239-2189d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711625 | |||||||
chr1:61711908 | C | CT | 29 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0035 others(26): Show |
30 | HG00280.hp1 HG00673.hp1 HG01175.hp1 others(27): Show |
intron_variant | MODIFIER | c.239-2472dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61711908 | |||||||
chr1:61712189 | G | A | 3 | a0001c0001t0001g0297 a0001c0001t0001g0302 a0001c0001t0001g0307 |
3 | HG01943.hp2 HG02273.hp1 HG02293.hp2 |
intron_variant | MODIFIER | c.239-2752C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712189 | |||||||
chr1:61712200 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.239-2763G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712200 | |||||||
chr1:61712389 | T | C | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-2952A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712389 | |||||||
chr1:61712422 | A | G | 2 | a0001c0001t0001g0285 a0001c0001t0001g0286 |
2 | HG00738.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.239-2985T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712422 | |||||||
chr1:61712767 | G | A | 1 | a0001c0001t0001g0109 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.239-3330C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712767 | |||||||
chr1:61712851 | T | C | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
125 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-3414A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712851 | |||||||
chr1:61712880 | A | C | 1 | a0001c0001t0001g0085 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.239-3443T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712880 | |||||||
chr1:61712912 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(320): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.239-3475T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712912 | |||||||
chr1:61712982 | C | T | 1 | a0001c0001t0003g0050 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.239-3545G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61712982 | |||||||
chr1:61713042 | C | T | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG00099.hp2 HG01175.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-3605G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713042 | |||||||
chr1:61713078 | G | A | 2 | a0001c0001t0001g0319 a0001c0001t0001g0320 |
2 | HG02451.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.239-3641C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713078 | |||||||
chr1:61713125 | G | A | 1 | a0001c0001t0002g0359 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.239-3688C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713125 | |||||||
chr1:61713151 | T | C | 3 | a0001c0001t0001g0272 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG01884.hp2 HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.239-3714A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713151 | |||||||
chr1:61713169 | C | CA | 10 | a0001c0001t0001g0086 a0001c0001t0001g0098 a0001c0001t0001g0237 others(7): Show |
10 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-3733dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713169 | |||||||
chr1:61713276 | A | G | 18 | a0001c0001t0001g0017 a0001c0001t0001g0246 a0001c0001t0001g0249 others(15): Show |
19 | HG01978.hp1 HG01981.hp2 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.239-3839T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713276 | |||||||
chr1:61713330 | T | C | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-3893A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713330 | |||||||
chr1:61713426 | C | T | 1 | a0001c0001t0001g0013 | 2 | HG02559.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.239-3989G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713426 | |||||||
chr1:61713444 | A | G | 1 | a0001c0001t0001g0086 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.239-4007T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713444 | |||||||
chr1:61713471 | C | T | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-4034G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713471 | |||||||
chr1:61713488 | C | A | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-4051G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713488 | |||||||
chr1:61713488 | C | CA | 27 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0027 others(24): Show |
29 | HG01099.hp1 HG01109.hp1 HG01346.hp1 others(26): Show |
intron_variant | MODIFIER | c.239-4052dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713488 | |||||||
chr1:61713488 | CA | C | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(113): Show |
121 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.239-4052delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713488 | |||||||
chr1:61713488 | CAAAAAAA others(3): Show |
C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.239-4061_239-4052d others(12): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713488 | |||||||
chr1:61713494 | A | C | 1 | a0001c0001t0001g0171 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.239-4057T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713494 | |||||||
chr1:61713500 | A | G | 2 | a0001c0001t0003g0056 a0001c0001t0003g0057 |
2 | HG00639.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.239-4063T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713500 | |||||||
chr1:61713524 | A | G | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(64): Show |
76 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.239-4087T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713524 | |||||||
chr1:61713777 | T | C | 3 | a0001c0001t0002g0359 a0001c0001t0002g0360 a0001c0001t0002g0363 |
3 | HG02630.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.239-4340A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713777 | |||||||
chr1:61713884 | C | CT | 24 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0031 others(21): Show |
25 | HG00099.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.239-4448dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713884 | |||||||
chr1:61713884 | C | CTT | 7 | a0001c0001t0001g0247 a0001c0001t0002g0345 a0001c0001t0002g0346 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-4449_239-4448d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713884 | |||||||
chr1:61713884 | CT | C | 108 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(105): Show |
113 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.239-4448delA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713884 | |||||||
chr1:61713884 | CTTTTTTT | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0017 a0001c0001t0001g0034 others(30): Show |
35 | HG00280.hp1 HG00673.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.239-4454_239-4448d others(9): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713884 | |||||||
chr1:61713912 | G | A | 1 | a0001c0001t0001g0075 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.239-4475C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713912 | |||||||
chr1:61713937 | G | A | 10 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(7): Show |
10 | HG01074.hp2 HG01109.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.239-4500C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713937 | |||||||
chr1:61713997 | G | A | 4 | a0001c0001t0001g0192 a0001c0001t0001g0193 a0001c0001t0001g0196 others(1): Show |
4 | HG00099.hp2 HG01175.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-4560C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61713997 | |||||||
chr1:61714044 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.239-4607G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714044 | |||||||
chr1:61714141 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.239-4704G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714141 | |||||||
chr1:61714175 | C | G | 360 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(357): Show |
384 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(381): Show |
intron_variant | MODIFIER | c.239-4738G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714175 | |||||||
chr1:61714191 | G | A | 3 | a0001c0001t0001g0194 a0001c0001t0001g0195 a0001c0001t0001g0215 |
3 | NA18979.hp2 NA18980.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.239-4754C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714191 | |||||||
chr1:61714268 | C | T | 3 | a0001c0001t0001g0296 a0001c0001t0001g0303 a0001c0001t0001g0308 |
3 | HG01243.hp1 HG04204.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.239-4831G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714268 | |||||||
chr1:61714370 | G | A | 4 | a0001c0001t0001g0197 a0001c0001t0001g0235 a0001c0001t0001g0243 others(1): Show |
4 | HG02109.hp2 HG02622.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-4933C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714370 | |||||||
chr1:61714397 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.239-4960G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714397 | |||||||
chr1:61714398 | G | A | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(18): Show |
28 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.239-4961C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714398 | |||||||
chr1:61714412 | G | A | 12 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(9): Show |
12 | HG01074.hp2 HG01109.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.239-4975C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714412 | |||||||
chr1:61714455 | T | G | 1 | a0001c0001t0001g0310 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.239-5018A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714455 | |||||||
chr1:61714498 | G | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(64): Show |
76 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.239-5061C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714498 | |||||||
chr1:61714577 | T | C | 1 | a0001c0001t0001g0196 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.239-5140A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714577 | |||||||
chr1:61714650 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.239-5213C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714650 | |||||||
chr1:61714683 | T | G | 2 | a0001c0001t0001g0324 a0001c0001t0001g0325 |
2 | HG01257.hp1 HG02258.hp2 |
intron_variant | MODIFIER | c.239-5246A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714683 | |||||||
chr1:61714701 | T | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.239-5264A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61714701 | |||||||
chr1:61715003 | G | A | 13 | a0001c0001t0002g0003 a0001c0001t0002g0348 a0001c0001t0002g0349 others(10): Show |
15 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-5566C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715003 | |||||||
chr1:61715030 | C | T | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.239-5593G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715030 | |||||||
chr1:61715103 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.239-5666T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715103 | |||||||
chr1:61715239 | G | C | 3 | a0001c0001t0001g0010 a0001c0001t0001g0165 a0001c0001t0001g0170 |
4 | HG00438.hp2 NA18944.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.239-5802C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715239 | |||||||
chr1:61715337 | G | A | 1 | a0001c0001t0001g0142 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.239-5900C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715337 | |||||||
chr1:61715341 | A | G | 1 | a0001c0001t0003g0055 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.239-5904T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715341 | |||||||
chr1:61715353 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.239-5916G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715353 | |||||||
chr1:61715477 | G | A | 1 | a0001c0001t0003g0048 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.239-6040C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715477 | |||||||
chr1:61715525 | G | A | 7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0056 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-6088C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715525 | |||||||
chr1:61715528 | G | C | 3 | a0001c0001t0001g0197 a0001c0001t0001g0235 a0001c0001t0001g0243 |
3 | HG02109.hp2 HG02622.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.239-6091C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715528 | |||||||
chr1:61715645 | C | CA | 61 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0061 others(58): Show |
61 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.239-6209dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715645 | C | CAA | 17 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0033 others(14): Show |
17 | HG00733.hp2 HG01358.hp2 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.239-6210_239-6209d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715645 | CA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(83): Show |
97 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.239-6209delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715645 | CAA | C | 17 | a0001c0001t0001g0018 a0001c0001t0001g0028 a0001c0001t0001g0034 others(14): Show |
18 | HG00639.hp2 HG01192.hp1 HG01943.hp2 others(15): Show |
intron_variant | MODIFIER | c.239-6210_239-6209d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715645 | CAAAA | C | 21 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(18): Show |
21 | HG00738.hp2 HG01109.hp2 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.239-6212_239-6209d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715645 | CAAAAA | C | 23 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(20): Show |
25 | HG01070.hp1 HG01074.hp2 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.239-6213_239-6209d others(7): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715645 | CAAAAAAA others(3): Show |
C | 3 | a0001c0001t0001g0016 a0001c0001t0001g0247 a0001c0001t0001g0248 |
4 | HG01099.hp1 HG01109.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.239-6218_239-6209d others(12): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715645 | |||||||
chr1:61715676 | C | A | 1 | a0001c0001t0001g0145 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.239-6239G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715676 | |||||||
chr1:61715684 | A | G | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.239-6247T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715684 | |||||||
chr1:61715697 | C | A | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-6260G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715697 | |||||||
chr1:61715791 | G | C | 7 | a0001c0001t0002g0345 a0001c0001t0002g0346 a0001c0001t0002g0347 others(4): Show |
7 | HG02280.hp1 HG02486.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.239-6354C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715791 | |||||||
chr1:61715862 | C | T | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.239-6425G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715862 | |||||||
chr1:61715934 | T | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.239-6497A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715934 | |||||||
chr1:61715965 | C | T | 7 | a0001c0001t0001g0275 a0001c0001t0001g0276 a0001c0001t0001g0277 others(4): Show |
7 | HG01074.hp2 HG01109.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-6528G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61715965 | |||||||
chr1:61716130 | G | T | 1 | a0001c0001t0001g0104 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.239-6693C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716130 | |||||||
chr1:61716237 | T | A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.239-6800A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716237 | |||||||
chr1:61716269 | C | T | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.239-6832G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716269 | |||||||
chr1:61716339 | C | A | 67 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(64): Show |
76 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(73): Show |
intron_variant | MODIFIER | c.239-6902G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716339 | |||||||
chr1:61716352 | C | T | 87 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(84): Show |
96 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.239-6915G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716352 | |||||||
chr1:61716383 | T | A | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
125 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.239-6946A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716383 | |||||||
chr1:61716417 | ATATAATT others(11): Show |
A | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-6998_239-6981d others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716417 | |||||||
chr1:61716420 | T | TAA | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18982.hp2 NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.239-6985_239-6984d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716420 | |||||||
chr1:61716430 | TAA | T | 5 | a0001c0001t0001g0100 a0001c0001t0001g0101 a0001c0001t0002g0359 others(2): Show |
5 | HG02630.hp1 HG03098.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.239-6995_239-6994d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716430 | |||||||
chr1:61716433 | G | T | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18982.hp2 NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.239-6996C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716433 | |||||||
chr1:61716435 | G | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18982.hp2 NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.239-6998C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716435 | |||||||
chr1:61716435 | G | GTATAATT others(21): Show |
7 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0056 others(4): Show |
7 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.239-7026_239-6999d others(30): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716435 | |||||||
chr1:61716438 | T | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18982.hp2 NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.239-7001A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716438 | |||||||
chr1:61716440 | A | C | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18982.hp2 NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.239-7003T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716440 | |||||||
chr1:61716443 | A | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.239-7006T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716443 | |||||||
chr1:61716449 | AATTTTAT others(41): Show |
A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.239-7060_239-7013d others(50): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716449 | |||||||
chr1:61716450 | ATT | A | 3 | a0001c0001t0001g0087 a0001c0001t0001g0102 a0001c0001t0001g0103 |
3 | NA18982.hp2 NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.239-7015_239-7014d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716450 | |||||||
chr1:61716461 | A | ATATATAA others(21): Show |
1 | a0001c0001t0001g0137 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.239-7052_239-7025d others(30): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716461 | |||||||
chr1:61716461 | A | G | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(42): Show |
52 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.239-7024T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716461 | |||||||
chr1:61716488 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.239-7051G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716488 | |||||||
chr1:61716489 | G | T | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.239-7052C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716489 | |||||||
chr1:61716499 | A | G | 2 | a0001c0001t0001g0100 a0001c0001t0001g0101 |
2 | NA18747.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.239-7062T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716499 | |||||||
chr1:61716535 | GTATAATT others(11): Show |
G | 6 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0079 others(3): Show |
6 | HG00735.hp1 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.239-7116_239-7099d others(20): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716535 | |||||||
chr1:61716572 | T | C | 1 | a0001c0001t0001g0316 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.239-7135A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716572 | |||||||
chr1:61716579 | TTA | T | 21 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(18): Show |
28 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.238+7132_238+7133d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716579 | |||||||
chr1:61716586 | T | C | 8 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(5): Show |
8 | HG02809.hp1 HG02818.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+7127A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716586 | |||||||
chr1:61716869 | C | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+6844G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716869 | |||||||
chr1:61716958 | C | G | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+6755G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61716958 | |||||||
chr1:61717014 | G | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.238+6699C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717014 | |||||||
chr1:61717074 | T | C | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(320): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.238+6639A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717074 | |||||||
chr1:61717115 | G | A | 2 | a0001c0001t0001g0065 a0001c0001t0001g0096 |
2 | HG02040.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.238+6598C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717115 | |||||||
chr1:61717130 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(83): Show |
95 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.238+6583A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717130 | |||||||
chr1:61717172 | C | G | 15 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(12): Show |
16 | HG00280.hp1 HG00673.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.238+6541G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717172 | |||||||
chr1:61717178 | C | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0025 others(9): Show |
14 | HG00438.hp2 HG01069.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.238+6535G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717178 | |||||||
chr1:61717202 | C | CA | 17 | a0001c0001t0001g0146 a0001c0001t0001g0226 a0001c0001t0001g0337 others(14): Show |
17 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.238+6510dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717202 | |||||||
chr1:61717202 | CA | C | 66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(63): Show |
75 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(72): Show |
intron_variant | MODIFIER | c.238+6510delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717202 | |||||||
chr1:61717205 | A | AAC | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+6507_238+6508i others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717205 | |||||||
chr1:61717206 | A | C | 31 | a0001c0001t0001g0008 a0001c0001t0001g0015 a0001c0001t0001g0061 others(28): Show |
33 | HG01081.hp1 HG01099.hp2 HG01934.hp2 others(30): Show |
intron_variant | MODIFIER | c.238+6507T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717206 | |||||||
chr1:61717207 | A | C | 110 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(107): Show |
117 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(114): Show |
intron_variant | MODIFIER | c.238+6506T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717207 | |||||||
chr1:61717208 | A | C | 2 | a0001c0001t0001g0275 a0001c0001t0001g0284 |
2 | HG02723.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.238+6505T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717208 | |||||||
chr1:61717225 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+6488C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717225 | |||||||
chr1:61717230 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238+6483A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717230 | |||||||
chr1:61717278 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+6435A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717278 | |||||||
chr1:61717284 | C | T | 1 | a0001c0001t0001g0166 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.238+6429G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717284 | |||||||
chr1:61717362 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.238+6351G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717362 | |||||||
chr1:61717431 | C | T | 1 | a0001c0001t0001g0250 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.238+6282G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717431 | |||||||
chr1:61717455 | T | C | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+6258A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717455 | |||||||
chr1:61717558 | G | A | 25 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(22): Show |
25 | HG00738.hp2 HG01074.hp2 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.238+6155C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717558 | |||||||
chr1:61717563 | G | GT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(21): Show |
31 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.238+6149dupA | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717563 | |||||||
chr1:61717599 | G | A | 1 | a0001c0001t0001g0244 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.238+6114C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717599 | |||||||
chr1:61717915 | G | A | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | HG01192.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+5798C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61717915 | |||||||
chr1:61718004 | G | A | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+5709C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718004 | |||||||
chr1:61718036 | C | T | 1 | a0002c0002t0004g0023 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.238+5677G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718036 | |||||||
chr1:61718287 | C | T | 1 | a0001c0001t0001g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.238+5426G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718287 | |||||||
chr1:61718290 | CA | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(83): Show |
95 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(92): Show |
intron_variant | MODIFIER | c.238+5422delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718290 | |||||||
chr1:61718381 | C | G | 1 | a0001c0001t0002g0359 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.238+5332G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718381 | |||||||
chr1:61718475 | T | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0147 a0001c0001t0001g0148 others(6): Show |
10 | NA18939.hp1 NA18940.hp2 NA18953.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+5238A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718475 | |||||||
chr1:61718536 | G | A | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+5177C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718536 | |||||||
chr1:61718628 | A | C | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+5085T>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718628 | |||||||
chr1:61718728 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.238+4985C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718728 | |||||||
chr1:61718791 | T | C | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.238+4922A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718791 | |||||||
chr1:61718869 | C | T | 3 | a0001c0001t0001g0016 a0001c0001t0001g0247 a0001c0001t0001g0248 |
4 | HG01099.hp1 HG01109.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.238+4844G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61718869 | |||||||
chr1:61719171 | T | C | 1 | a0001c0001t0001g0266 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.238+4542A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719171 | |||||||
chr1:61719219 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.238+4494C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719219 | |||||||
chr1:61719232 | T | C | 1 | a0001c0001t0002g0358 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.238+4481A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719232 | |||||||
chr1:61719375 | A | G | 8 | a0001c0001t0001g0083 a0001c0001t0001g0084 a0001c0001t0001g0085 others(5): Show |
8 | NA18612.hp2 NA18943.hp2 NA18944.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+4338T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719375 | |||||||
chr1:61719409 | C | CAG | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
128 | HG00099.hp2 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.238+4302_238+4303d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719409 | |||||||
chr1:61719409 | C | CAGAG | 9 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(6): Show |
9 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.238+4300_238+4303d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719409 | |||||||
chr1:61719409 | C | CAGAGAG | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+4298_238+4303d others(8): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719409 | |||||||
chr1:61719409 | CAGAG | C | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+4300_238+4303d others(6): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719409 | |||||||
chr1:61719455 | T | G | 120 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
125 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(122): Show |
intron_variant | MODIFIER | c.238+4258A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719455 | |||||||
chr1:61719515 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.238+4198C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719515 | |||||||
chr1:61719542 | G | C | 2 | a0002c0002t0001g0021 a0002c0002t0001g0022 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.238+4171C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719542 | |||||||
chr1:61719602 | C | T | 1 | a0001c0001t0001g0217 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.238+4111G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719602 | |||||||
chr1:61719604 | T | C | 5 | a0001c0001t0002g0354 a0001c0001t0002g0355 a0001c0001t0002g0356 others(2): Show |
5 | HG01255.hp2 HG02055.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.238+4109A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719604 | |||||||
chr1:61719638 | A | G | 15 | a0001c0001t0001g0027 a0001c0001t0001g0062 a0001c0001t0001g0272 others(12): Show |
15 | HG00738.hp2 HG01192.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.238+4075T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719638 | |||||||
chr1:61719686 | G | C | 1 | a0001c0001t0001g0317 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.238+4027C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719686 | |||||||
chr1:61719718 | C | G | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
117 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(114): Show |
intron_variant | MODIFIER | c.238+3995G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719718 | |||||||
chr1:61719838 | G | A | 1 | a0001c0001t0001g0292 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.238+3875C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719838 | |||||||
chr1:61719843 | G | T | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+3870C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719843 | |||||||
chr1:61719882 | T | C | 3 | a0001c0001t0001g0031 a0001c0001t0001g0032 a0001c0001t0001g0033 |
3 | NA19067.hp1 NA19070.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.238+3831A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61719882 | |||||||
chr1:61720030 | C | T | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238+3683G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720030 | |||||||
chr1:61720236 | C | G | 1 | a0001c0001t0001g0246 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.238+3477G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720236 | |||||||
chr1:61720293 | G | A | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+3420C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720293 | |||||||
chr1:61720418 | T | C | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+3295A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720418 | |||||||
chr1:61720443 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.238+3270A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720443 | |||||||
chr1:61720447 | T | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(320): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.238+3266A>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720447 | |||||||
chr1:61720485 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.238+3228C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720485 | |||||||
chr1:61720600 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.238+3113G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720600 | |||||||
chr1:61720684 | T | C | 1 | a0001c0001t0001g0228 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.238+3029A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720684 | |||||||
chr1:61720751 | A | G | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+2962T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720751 | |||||||
chr1:61720762 | C | T | 1 | a0001c0001t0001g0245 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.238+2951G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720762 | |||||||
chr1:61720763 | A | G | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+2950T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61720763 | |||||||
chr1:61721052 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(42): Show |
52 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.238+2661G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721052 | |||||||
chr1:61721059 | C | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG01167.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.238+2654G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721059 | |||||||
chr1:61721065 | C | A | 6 | a0001c0001t0001g0309 a0001c0001t0001g0310 a0001c0001t0001g0311 others(3): Show |
6 | HG02027.hp2 HG02132.hp2 NA18939.hp2 others(3): Show |
intron_variant | MODIFIER | c.238+2648G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721065 | |||||||
chr1:61721074 | A | T | 1 | a0001c0001t0001g0294 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.238+2639T>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721074 | |||||||
chr1:61721279 | C | T | 7 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(4): Show |
7 | HG00738.hp2 HG02615.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.238+2434G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721279 | |||||||
chr1:61721361 | G | A | 10 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(7): Show |
10 | HG00738.hp2 HG01192.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+2352C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721361 | |||||||
chr1:61721395 | A | G | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.238+2318T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721395 | |||||||
chr1:61721400 | G | C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+2313C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721400 | |||||||
chr1:61721419 | A | G | 323 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(320): Show |
344 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(341): Show |
intron_variant | MODIFIER | c.238+2294T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721419 | |||||||
chr1:61721510 | C | A | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+2203G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721510 | |||||||
chr1:61721541 | CA | C | 277 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
289 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(286): Show |
intron_variant | MODIFIER | c.238+2171delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721541 | |||||||
chr1:61721548 | AAAAAAAA others(2): Show |
A | 14 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0348 others(11): Show |
16 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.238+2156_238+2164d others(11): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721548 | |||||||
chr1:61721587 | T | C | 3 | a0001c0001t0002g0359 a0001c0001t0002g0360 a0001c0001t0002g0363 |
3 | HG02630.hp1 HG03098.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.238+2126A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721587 | |||||||
chr1:61721913 | G | A | 113 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(110): Show |
117 | HG00423.hp2 HG00438.hp1 HG00673.hp2 others(114): Show |
intron_variant | MODIFIER | c.238+1800C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721913 | |||||||
chr1:61721935 | C | A | 3 | a0001c0001t0004g0282 a0001c0001t0004g0283 a0002c0002t0004g0023 |
3 | HG02615.hp1 HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.238+1778G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721935 | |||||||
chr1:61721951 | T | TA | 121 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(118): Show |
129 | HG00099.hp2 HG00438.hp2 HG00673.hp1 others(126): Show |
intron_variant | MODIFIER | c.238+1761dupT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721951 | |||||||
chr1:61721951 | T | TAA | 27 | a0001c0001t0001g0230 a0001c0001t0001g0231 a0001c0001t0001g0232 others(24): Show |
27 | HG00423.hp1 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.238+1760_238+1761d others(4): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721951 | |||||||
chr1:61721951 | TA | T | 37 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(34): Show |
44 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(41): Show |
intron_variant | MODIFIER | c.238+1761delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721951 | |||||||
chr1:61721951 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0005g0271 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.238+1749_238+1761d others(15): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721951 | |||||||
chr1:61721951 | TAAAAAAA others(8): Show |
T | 1 | a0001c0001t0002g0344 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.238+1747_238+1761d others(17): Show |
TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61721951 | |||||||
chr1:61722010 | G | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(7): Show |
10 | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.238+1703C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722010 | |||||||
chr1:61722099 | T | C | 3 | a0001c0001t0001g0291 a0001c0001t0001g0292 a0001c0001t0001g0293 |
3 | HG01192.hp1 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.238+1614A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722099 | |||||||
chr1:61722155 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0016 a0001c0001t0001g0017 others(34): Show |
40 | HG00280.hp1 HG00673.hp1 HG01099.hp1 others(37): Show |
intron_variant | MODIFIER | c.238+1558C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722155 | |||||||
chr1:61722283 | G | A | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+1430C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722283 | |||||||
chr1:61722544 | C | T | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.238+1169G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722544 | |||||||
chr1:61722682 | G | A | 1 | a0001c0001t0001g0270 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.238+1031C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722682 | |||||||
chr1:61722690 | T | A | 20 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(17): Show |
27 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.238+1023A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722690 | |||||||
chr1:61722717 | T | C | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.238+996A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722717 | |||||||
chr1:61722760 | C | T | 45 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(42): Show |
52 | HG00099.hp1 HG00280.hp2 HG00738.hp2 others(49): Show |
intron_variant | MODIFIER | c.238+953G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722760 | |||||||
chr1:61722892 | T | C | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.238+821A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722892 | |||||||
chr1:61722946 | C | A | 84 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(81): Show |
93 | HG00099.hp1 HG00280.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.238+767G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61722946 | |||||||
chr1:61723283 | G | C | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.238+430C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61723283 | |||||||
chr1:61723290 | T | C | 2 | a0001c0001t0004g0282 a0001c0001t0004g0283 |
2 | HG02818.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.238+423A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61723290 | |||||||
chr1:61723307 | G | T | 26 | a0001c0001t0001g0018 a0001c0001t0001g0294 a0001c0001t0001g0295 others(23): Show |
27 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.238+406C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61723307 | |||||||
chr1:61723548 | G | C | 10 | a0001c0001t0001g0284 a0001c0001t0001g0285 a0001c0001t0001g0286 others(7): Show |
10 | HG00738.hp2 HG01192.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.238+165C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 2/6 | chr1 | 61723548 | |||||||
chr1:61723869 | T | C | 28 | a0001c0001t0001g0018 a0001c0001t0001g0294 a0001c0001t0001g0295 others(25): Show |
29 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.165-83A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61723869 | |||||||
chr1:61724184 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-398C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724184 | |||||||
chr1:61724185 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-399A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724185 | |||||||
chr1:61724186 | G | C | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-400C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724186 | |||||||
chr1:61724189 | T | A | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-403A>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724189 | |||||||
chr1:61724192 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-406A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724192 | |||||||
chr1:61724194 | G | A | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-408C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724194 | |||||||
chr1:61724195 | T | C | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-409A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724195 | |||||||
chr1:61724199 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-413C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724199 | |||||||
chr1:61724200 | G | T | 1 | a0001c0001t0001g0061 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.165-414C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724200 | |||||||
chr1:61724201 | G | T | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(15): Show |
25 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.165-415C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724201 | |||||||
chr1:61724239 | C | T | 1 | a0002c0002t0001g0021 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.165-453G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724239 | |||||||
chr1:61724262 | G | A | 1 | a0001c0001t0001g0321 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.165-476C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724262 | |||||||
chr1:61724270 | T | C | 18 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0019 others(15): Show |
25 | HG00099.hp1 HG00280.hp2 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.165-484A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724270 | |||||||
chr1:61724305 | T | C | 1 | a0001c0001t0001g0335 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.165-519A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724305 | |||||||
chr1:61724343 | G | T | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.165-557C>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724343 | |||||||
chr1:61724350 | C | A | 1 | a0001c0001t0001g0336 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.165-564G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724350 | |||||||
chr1:61724358 | G | A | 8 | a0001c0001t0003g0053 a0001c0001t0003g0054 a0001c0001t0003g0055 others(5): Show |
8 | HG00639.hp1 HG01243.hp2 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.165-572C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724358 | |||||||
chr1:61724529 | T | C | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.164+428A>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724529 | |||||||
chr1:61724554 | G | C | 7 | a0001c0001t0001g0337 a0001c0001t0001g0338 a0001c0001t0001g0339 others(4): Show |
7 | HG02809.hp1 HG02895.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.164+403C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724554 | |||||||
chr1:61724634 | G | C | 2 | a0001c0001t0003g0059 a0001c0001t0003g0060 |
2 | HG01243.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.164+323C>G | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724634 | |||||||
chr1:61724644 | C | T | 18 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0001c0001t0003g0045 others(15): Show |
18 | HG00639.hp1 HG01243.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.164+313G>A | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724644 | |||||||
chr1:61724662 | A | G | 10 | a0001c0001t0001g0004 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
11 | HG00673.hp1 NA18747.hp2 NA18946.hp2 others(8): Show |
intron_variant | MODIFIER | c.164+295T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724662 | |||||||
chr1:61724707 | GA | G | 5 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0031 others(2): Show |
5 | NA18962.hp1 NA19011.hp1 NA19067.hp1 others(2): Show |
intron_variant | MODIFIER | c.164+249delT | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724707 | |||||||
chr1:61724736 | G | A | 21 | a0001c0001t0002g0003 a0001c0001t0002g0344 a0001c0001t0002g0345 others(18): Show |
23 | HG01070.hp1 HG01255.hp2 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.164+221C>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724736 | |||||||
chr1:61724757 | A | G | 1 | a0001c0001t0001g0028 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.164+200T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724757 | |||||||
chr1:61724765 | C | G | 1 | a0001c0001t0001g0027 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.164+192G>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724765 | |||||||
chr1:61724791 | A | G | 2 | a0001c0001t0001g0025 a0001c0001t0001g0026 |
2 | HG02735.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.164+166T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724791 | |||||||
chr1:61724840 | A | G | 1 | a0001c0001t0001g0024 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.164+117T>C | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724840 | |||||||
chr1:61724873 | C | A | 1 | a0001c0001t0001g0364 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.164+84G>T | TM2D1 | ENSG00000162604.13 | transcript | ENST00000606498.5 | protein_coding | 1/6 | chr1 | 61724873 |