Item | Value |
---|---|
geneid | 23158 |
ensemblid | ENSG00000109436.8 |
hgncid | 21710 |
symbol | TBC1D9 |
name | TBC1 domain family member 9 |
refseq_nuc | NM_015130.3 |
refseq_prot | NP_055945.2 |
ensembl_nuc | ENST00000442267.3 |
ensembl_prot | ENSP00000411197.2 |
mane_status | MANE Select |
chr | chr4 |
start | 140620782 |
end | 140756385 |
strand | - |
ver | v1.2 |
region | chr4:140620782-140756385 |
region5000 | chr4:140615782-140761385 |
regionname0 | TBC1D9_chr4_140620782_140756385 |
regionname5000 | TBC1D9_chr4_140615782_140761385 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1266 | 291 | 86 | 63 | 104 | 10 | 26 | 80 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | MWVNP others(1261): Show |
chr4 | 140615782 | 140761385 |
a0002 | 0/0 | 1266 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | MWVNP others(1261): Show |
chr4 | 140615782 | 140761385 |
a0003 | 0/0 | 1266 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | MWVNP others(1261): Show |
chr4 | 140615782 | 140761385 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 3798 | 125 | 37 | 26 | 38 | 6 | 17 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0002 | 0/0 | 3798 | 59 | 14 | 21 | 17 | 3 | 4 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0003 | 0/0 | 3798 | 27 | 2 | 3 | 20 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0004 | 0/0 | 3798 | 24 | 7 | 6 | 9 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0005 | 0/0 | 3798 | 15 | 11 | 2 | 0 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0006 | 1/0 | 3798 | 12 | 1 | 1 | 9 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0007 | 0/0 | 3798 | 8 | 0 | 0 | 8 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0008 | 0/0 | 3798 | 8 | 7 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0010 | 0/0 | 3798 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0011 | 0/0 | 3798 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0012 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0013 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0014 | 0/0 | 3798 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0015 | 0/0 | 3798 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0016 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0017 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0018 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0020 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0001c0021 | 0/0 | 3798 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0002c0009 | 0/0 | 3798 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 | ||
a0003c0019 | 0/0 | 3798 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | ATGTG others(3793): Show |
chr4 | 140615782 | 140761385 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5554 | 94 | 27 | 21 | 26 | 5 | 15 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0002 | 0/1 | 5554 | 12 | 6 | 1 | 2 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0003 | 0/0 | 5554 | 8 | 0 | 4 | 3 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0004 | 0/0 | 5554 | 5 | 0 | 0 | 5 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0005 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0006 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0010 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0014 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0016 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0001t0017 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0002t0001 | 0/0 | 5554 | 46 | 11 | 13 | 16 | 3 | 3 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0002t0002 | 0/0 | 5554 | 5 | 1 | 3 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0002t0003 | 0/0 | 5554 | 4 | 1 | 3 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0002t0006 | 0/0 | 5554 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0002t0013 | 0/0 | 5554 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0002t0015 | 0/0 | 5554 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0003t0001 | 0/0 | 5554 | 25 | 1 | 3 | 19 | 1 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0003t0003 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0003t0007 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0004t0001 | 0/0 | 5554 | 19 | 5 | 5 | 7 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0004t0002 | 0/0 | 5554 | 4 | 1 | 1 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0004t0005 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0005t0001 | 0/0 | 5554 | 10 | 10 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0005t0002 | 0/0 | 5554 | 4 | 0 | 2 | 0 | 0 | 2 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0005t0009 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0006t0001 | 1/0 | 5554 | 11 | 1 | 1 | 8 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0006t0007 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0007t0001 | 0/0 | 5554 | 7 | 0 | 0 | 7 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0007t0007 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0008t0001 | 0/0 | 5554 | 4 | 4 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0008t0002 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0008t0003 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0008t0005 | 0/0 | 5554 | 2 | 1 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0010t0001 | 0/0 | 5554 | 2 | 0 | 0 | 2 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0011t0001 | 0/0 | 5554 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0012t0008 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0013t0011 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0014t0001 | 0/0 | 5554 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0015t0002 | 0/0 | 5554 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0016t0012 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0017t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0018t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0020t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0001c0021t0001 | 0/0 | 5554 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0002c0009t0002 | 0/0 | 5554 | 6 | 0 | 0 | 6 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
a0003c0019t0002 | 0/0 | 5554 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | CTCCT others(5549): Show |
chr4 | 140615782 | 140761385 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0002 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0002g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0003g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0004g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0004g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0004g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0004g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0004g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0010g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0016g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0001t0017g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0002g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0002g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0003g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0003g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0003g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0006g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0006g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0013g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0002t0015g0280 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0003g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0003t0007g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0002g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0004t0005g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0005t0009g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0006t0007g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0007t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0005g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0008t0005g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0010t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0010t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0011t0001g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0012t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0013t0011g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0014t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0015t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0016t0012g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0017t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0018t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0020t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0001c0021t0001g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0002c0009t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0002c0009t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0002c0009t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0002c0009t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0002c0009t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0002c0009t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
a0003c0019t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0003 | t0001 | g0097 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00099 | hp2 | a0001 | c0002 | t0001 | g0200 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0039 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0189 | EUR | GBR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00408 | hp2 | a0001 | c0004 | t0001 | g0120 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0038 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00544 | hp1 | a0001 | c0003 | t0001 | g0068 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00558 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00558 | hp2 | a0001 | c0004 | t0001 | g0105 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00609 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00621 | hp1 | a0001 | c0003 | t0001 | g0042 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00639 | hp1 | a0001 | c0005 | t0002 | g0128 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00639 | hp2 | a0001 | c0002 | t0002 | g0088 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00642 | hp2 | a0001 | c0003 | t0001 | g0069 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00673 | hp1 | a0001 | c0002 | t0001 | g0207 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00673 | hp2 | a0001 | c0003 | t0001 | g0075 | EAS | CHS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00733 | hp1 | a0001 | c0002 | t0001 | g0193 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00735 | hp1 | a0001 | c0002 | t0006 | g0165 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00735 | hp2 | a0001 | c0004 | t0002 | g0127 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00741 | hp1 | a0001 | c0004 | t0001 | g0136 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01069 | hp1 | a0001 | c0004 | t0001 | g0124 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01069 | hp2 | a0001 | c0002 | t0001 | g0209 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01070 | hp1 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01070 | hp2 | a0001 | c0001 | t0003 | g0288 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01071 | hp1 | a0001 | c0004 | t0001 | g0126 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01071 | hp2 | a0001 | c0001 | t0003 | g0287 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01074 | hp1 | a0003 | c0019 | t0002 | g0125 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0281 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01081 | hp1 | a0001 | c0002 | t0003 | g0275 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0198 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01167 | hp1 | a0001 | c0002 | t0001 | g0247 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01167 | hp2 | a0001 | c0003 | t0001 | g0023 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01169 | hp1 | a0001 | c0002 | t0001 | g0197 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01169 | hp2 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0244 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0246 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01256 | hp1 | a0001 | c0011 | t0001 | g0001 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01256 | hp2 | a0001 | c0004 | t0001 | g0173 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01257 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01258 | hp2 | a0001 | c0011 | t0001 | g0001 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01261 | hp2 | a0001 | c0008 | t0005 | g0242 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01346 | hp2 | a0001 | c0002 | t0002 | g0226 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01358 | hp1 | a0001 | c0002 | t0001 | g0248 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01361 | hp1 | a0001 | c0002 | t0003 | g0283 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01361 | hp2 | a0001 | c0014 | t0001 | g0089 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0196 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0185 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0199 | EUR | IBS | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01884 | hp1 | a0001 | c0002 | t0006 | g0099 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01891 | hp2 | a0001 | c0006 | t0001 | g0256 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0257 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01928 | hp2 | a0001 | c0002 | t0001 | g0138 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01943 | hp1 | a0001 | c0003 | t0001 | g0022 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01943 | hp2 | a0001 | c0004 | t0001 | g0137 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0278 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01975 | hp2 | a0001 | c0002 | t0002 | g0232 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0263 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02056 | hp1 | a0001 | c0004 | t0001 | g0169 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02083 | hp1 | a0001 | c0003 | t0001 | g0074 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02083 | hp2 | a0001 | c0004 | t0001 | g0225 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0115 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02145 | hp2 | a0001 | c0002 | t0001 | g0243 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02155 | hp2 | a0001 | c0006 | t0007 | g0228 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02165 | hp1 | a0001 | c0003 | t0001 | g0217 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02165 | hp2 | a0001 | c0001 | t0003 | g0286 | EAS | CDX | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02258 | hp1 | a0001 | c0017 | t0001 | g0159 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02258 | hp2 | a0001 | c0001 | t0017 | g0297 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02280 | hp2 | a0001 | c0008 | t0001 | g0180 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02300 | hp1 | a0001 | c0005 | t0002 | g0131 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02300 | hp2 | a0001 | c0002 | t0013 | g0252 | AMR | PEL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0267 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02451 | hp2 | a0001 | c0008 | t0001 | g0184 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02523 | hp1 | a0001 | c0002 | t0001 | g0233 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | KHV | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02572 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0092 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02615 | hp2 | a0001 | c0003 | t0003 | g0285 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0100 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02622 | hp2 | a0001 | c0005 | t0001 | g0129 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02630 | hp1 | a0001 | c0005 | t0001 | g0132 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0270 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02647 | hp2 | a0001 | c0008 | t0002 | g0187 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02698 | hp2 | a0001 | c0001 | t0003 | g0277 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0135 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02723 | hp1 | a0001 | c0001 | t0014 | g0284 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02723 | hp2 | a0001 | c0005 | t0009 | g0005 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02735 | hp1 | a0001 | c0002 | t0001 | g0174 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02735 | hp2 | a0001 | c0004 | t0001 | g0111 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02809 | hp1 | a0001 | c0008 | t0005 | g0179 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02886 | hp1 | a0001 | c0013 | t0011 | g0116 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02886 | hp2 | a0001 | c0001 | t0002 | g0157 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02895 | hp1 | a0001 | c0001 | t0006 | g0142 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0158 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0269 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02896 | hp2 | a0001 | c0004 | t0005 | g0266 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02897 | hp1 | a0001 | c0005 | t0001 | g0146 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0268 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02922 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0172 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02970 | hp1 | a0001 | c0002 | t0001 | g0098 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03041 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03041 | hp2 | a0001 | c0008 | t0003 | g0276 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03130 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0194 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03139 | hp1 | a0001 | c0008 | t0001 | g0186 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03139 | hp2 | a0001 | c0004 | t0001 | g0143 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0210 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03225 | hp1 | a0001 | c0012 | t0008 | g0147 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0274 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03453 | hp2 | a0001 | c0005 | t0001 | g0160 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0229 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03491 | hp1 | a0001 | c0005 | t0002 | g0104 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03492 | hp2 | a0001 | c0005 | t0002 | g0103 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03516 | hp1 | a0001 | c0004 | t0002 | g0261 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03688 | hp2 | a0001 | c0003 | t0001 | g0009 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG04184 | hp2 | a0001 | c0002 | t0001 | g0245 | SAS | BEB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0067 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0112 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG04228 | hp1 | a0001 | c0002 | t0015 | g0280 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18522 | hp2 | a0001 | c0005 | t0001 | g0130 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18943 | hp1 | a0001 | c0003 | t0001 | g0240 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18943 | hp2 | a0001 | c0003 | t0001 | g0072 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18944 | hp2 | a0001 | c0006 | t0001 | g0236 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18948 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18953 | hp1 | a0001 | c0002 | t0001 | g0253 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18963 | hp1 | a0001 | c0001 | t0004 | g0296 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18963 | hp2 | a0001 | c0007 | t0001 | g0220 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18964 | hp1 | a0001 | c0004 | t0002 | g0018 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18966 | hp1 | a0002 | c0009 | t0002 | g0046 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18966 | hp2 | a0001 | c0006 | t0001 | g0213 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18967 | hp2 | a0001 | c0006 | t0001 | g0258 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18969 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18969 | hp2 | a0001 | c0003 | t0001 | g0043 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18971 | hp1 | a0001 | c0003 | t0001 | g0041 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18971 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18972 | hp2 | a0001 | c0006 | t0001 | g0262 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18973 | hp1 | a0001 | c0007 | t0001 | g0171 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18973 | hp2 | a0001 | c0002 | t0001 | g0214 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18975 | hp1 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18979 | hp2 | a0001 | c0006 | t0001 | g0264 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18981 | hp1 | a0001 | c0007 | t0007 | g0107 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18982 | hp1 | a0002 | c0009 | t0002 | g0037 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18984 | hp1 | a0001 | c0007 | t0001 | g0239 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18984 | hp2 | a0002 | c0009 | t0002 | g0048 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18987 | hp1 | a0001 | c0003 | t0001 | g0084 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18988 | hp1 | a0002 | c0009 | t0002 | g0121 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18988 | hp2 | a0001 | c0004 | t0001 | g0047 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18989 | hp1 | a0001 | c0003 | t0007 | g0013 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18989 | hp2 | a0001 | c0007 | t0001 | g0219 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18990 | hp1 | a0001 | c0007 | t0001 | g0119 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18991 | hp1 | a0001 | c0003 | t0001 | g0056 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18991 | hp2 | a0001 | c0001 | t0016 | g0295 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18993 | hp2 | a0001 | c0007 | t0001 | g0255 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0205 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA18995 | hp2 | a0001 | c0015 | t0002 | g0085 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19000 | hp1 | a0001 | c0003 | t0001 | g0081 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19009 | hp1 | a0001 | c0006 | t0001 | g0206 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19009 | hp2 | a0001 | c0001 | t0003 | g0279 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19011 | hp1 | a0001 | c0007 | t0001 | g0230 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0289 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19012 | hp2 | a0001 | c0003 | t0001 | g0254 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0141 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19043 | hp1 | a0001 | c0008 | t0001 | g0241 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19056 | hp1 | a0001 | c0002 | t0001 | g0095 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19056 | hp2 | a0001 | c0010 | t0001 | g0260 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19057 | hp2 | a0001 | c0010 | t0001 | g0191 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19063 | hp1 | a0002 | c0009 | t0002 | g0040 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19063 | hp2 | a0001 | c0002 | t0001 | g0235 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19064 | hp1 | a0001 | c0004 | t0001 | g0108 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0221 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19066 | hp1 | a0001 | c0002 | t0001 | g0211 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19066 | hp2 | a0001 | c0003 | t0001 | g0078 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0294 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19067 | hp2 | a0001 | c0006 | t0001 | g0259 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19070 | hp1 | a0001 | c0003 | t0001 | g0086 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19070 | hp2 | a0001 | c0002 | t0001 | g0231 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19074 | hp2 | a0001 | c0002 | t0001 | g0190 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19079 | hp1 | a0001 | c0001 | t0004 | g0293 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19079 | hp2 | a0001 | c0006 | t0001 | g0030 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19083 | hp1 | a0001 | c0001 | t0010 | g0055 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0292 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19084 | hp1 | a0001 | c0003 | t0001 | g0079 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19084 | hp2 | a0001 | c0004 | t0001 | g0122 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0291 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19088 | hp2 | a0001 | c0004 | t0002 | g0017 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19091 | hp1 | a0001 | c0003 | t0001 | g0025 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19091 | hp2 | a0002 | c0009 | t0002 | g0049 | EAS | JPT | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19240 | hp1 | a0001 | c0004 | t0001 | g0153 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0134 | AFR | YRI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ASW | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20129 | hp2 | a0001 | c0021 | t0001 | g0265 | AFR | ASW | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0222 | EUR | TSI | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0058 | SAS | GIH | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20905 | hp2 | a0001 | c0004 | t0001 | g0114 | SAS | GIH | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01123 | hp1 | a0001 | c0002 | t0001 | g0234 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG01123 | hp2 | a0001 | c0006 | t0001 | g0019 | AMR | CLM | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02486 | hp1 | a0001 | c0004 | t0001 | g0273 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02486 | hp2 | a0001 | c0002 | t0001 | g0101 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02559 | hp1 | a0001 | c0016 | t0012 | g0272 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG02559 | hp2 | a0001 | c0002 | t0003 | g0290 | AFR | ACB | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0087 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG03471 | hp2 | a0001 | c0002 | t0001 | g0201 | AFR | MSL | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG06807 | hp1 | a0001 | c0020 | t0001 | g0188 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA20300 | hp2 | a0001 | c0005 | t0001 | g0133 | AFR | USA | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
NA21309 | hp2 | a0001 | c0018 | t0001 | g0175 | AFR | LWK | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0002 | REF | REF | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
homoSapiens | grch38p0 | a0001 | c0006 | t0001 | g0102 | REF | REF | TBC1D9_chr4_140615782_140761385 | TBC1D9 | chr4 | 140615782 | 140761385 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140622761 | C | T | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.3235G>A | p.Gly1079Arg | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3575/5554 | 3235/3801 | 1079/1266 | chr4 | 140622761 | |||
chr4:140622862 | T | C | 1 | a0002 | 6 | NA18966.hp1 NA18982.hp1 NA18984.hp2 others(3): Show |
missense_variant | MODERATE | c.3134A>G | p.Asn1045Ser | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3474/5554 | 3134/3801 | 1045/1266 | chr4 | 140622862 | |||
chr4:140662084 | G | A | 1 | a0003 | 1 | HG01074.hp1 | missense_variant | MODERATE | c.1612C>T | p.His538Tyr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/21 | 1952/5554 | 1612/3801 | 538/1266 | chr4 | 140662084 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140622435 | C | T | 1 | a0001c0016 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.3561G>A | p.Thr1187Thr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3901/5554 | 3561/3801 | 1187/1266 | chr4 | 140622435 | |||
chr4:140622741 | C | T | 2 | a0001c0013 a0001c0017 |
2 | HG02258.hp1 HG02886.hp1 |
synonymous_variant | LOW | c.3255G>A | p.Pro1085Pro | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3595/5554 | 3255/3801 | 1085/1266 | chr4 | 140622741 | |||
chr4:140622810 | C | T | 1 | a0001c0012 | 1 | HG03225.hp1 | synonymous_variant | LOW | c.3186G>A | p.Glu1062Glu | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3526/5554 | 3186/3801 | 1062/1266 | chr4 | 140622810 | |||
chr4:140622843 | G | A | 15 | a0001c0001 a0001c0002 a0001c0004 others(12): Show |
246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
synonymous_variant | LOW | c.3153C>T | p.His1051His | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 3493/5554 | 3153/3801 | 1051/1266 | chr4 | 140622843 | |||
chr4:140639342 | C | T | 1 | a0001c0016 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.2424G>A | p.Thr808Thr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 14/21 | 2764/5554 | 2424/3801 | 808/1266 | chr4 | 140639342 | |||
chr4:140639423 | G | A | 1 | a0001c0018 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.2343C>T | p.Phe781Phe | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 14/21 | 2683/5554 | 2343/3801 | 781/1266 | chr4 | 140639423 | |||
chr4:140657802 | C | T | 1 | a0001c0015 | 1 | NA18995.hp2 | synonymous_variant | LOW | c.1932G>A | p.Val644Val | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 12/21 | 2272/5554 | 1932/3801 | 644/1266 | chr4 | 140657802 | |||
chr4:140662022 | C | T | 3 | a0001c0005 a0001c0008 a0001c0014 |
24 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(21): Show |
synonymous_variant | LOW | c.1674G>A | p.Glu558Glu | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/21 | 2014/5554 | 1674/3801 | 558/1266 | chr4 | 140662022 | |||
chr4:140668981 | C | T | 1 | a0001c0011 | 2 | HG01256.hp1 HG01258.hp2 |
synonymous_variant | LOW | c.1524G>A | p.Thr508Thr | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/21 | 1864/5554 | 1524/3801 | 508/1266 | chr4 | 140668981 | |||
chr4:140676972 | C | T | 6 | a0001c0004 a0001c0007 a0001c0012 others(3): Show |
41 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(38): Show |
synonymous_variant | LOW | c.981G>A | p.Gln327Gln | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/21 | 1321/5554 | 981/3801 | 327/1266 | chr4 | 140676972 | |||
chr4:140679166 | A | G | 15 | a0001c0001 a0001c0003 a0001c0004 others(12): Show |
213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
synonymous_variant | LOW | c.627T>C | p.Leu209Leu | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/21 | 967/5554 | 627/3801 | 209/1266 | chr4 | 140679166 | |||
chr4:140679760 | A | G | 1 | a0001c0010 | 2 | NA19056.hp2 NA19057.hp2 |
synonymous_variant | LOW | c.444T>C | p.Phe148Phe | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/21 | 784/5554 | 444/3801 | 148/1266 | chr4 | 140679760 | |||
chr4:140701511 | G | A | 2 | a0001c0020 a0001c0021 |
2 | HG06807.hp1 NA20129.hp2 |
synonymous_variant | LOW | c.234C>T | p.Ile78Ile | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/21 | 574/5554 | 234/3801 | 78/1266 | chr4 | 140701511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140621012 | C | T | 1 | a0001c0013t0011 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1183G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 1183 | chr4 | 140621012 | ||||||
chr4:140621116 | G | C | 2 | a0001c0001t0006 a0001c0002t0006 |
3 | HG00735.hp1 HG01884.hp1 HG02895.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1079C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 1079 | chr4 | 140621116 | ||||||
chr4:140621218 | T | G | 1 | a0001c0016t0012 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*977A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 977 | chr4 | 140621218 | ||||||
chr4:140621336 | C | G | 9 | a0001c0001t0002 a0001c0002t0002 a0001c0002t0015 others(6): Show |
34 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*859G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 859 | chr4 | 140621336 | ||||||
chr4:140621604 | C | T | 4 | a0001c0001t0005 a0001c0001t0014 a0001c0004t0005 others(1): Show |
5 | HG01261.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*591G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 591 | chr4 | 140621604 | ||||||
chr4:140621731 | C | T | 1 | a0001c0001t0010 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*464G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 464 | chr4 | 140621731 | ||||||
chr4:140621900 | A | C | 1 | a0001c0005t0009 | 1 | HG02723.hp2 | 3_prime_UTR_variant | MODIFIER | c.*295T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 295 | chr4 | 140621900 | ||||||
chr4:140621908 | A | G | 1 | a0001c0012t0008 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*287T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 287 | chr4 | 140621908 | ||||||
chr4:140621985 | T | A | 3 | a0001c0003t0007 a0001c0006t0007 a0001c0007t0007 |
3 | HG02155.hp2 NA18981.hp1 NA18989.hp1 |
3_prime_UTR_variant | MODIFIER | c.*210A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 210 | chr4 | 140621985 | ||||||
chr4:140622046 | T | C | 1 | a0001c0002t0013 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*149A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 149 | chr4 | 140622046 | ||||||
chr4:140622082 | C | T | 1 | a0001c0001t0016 | 1 | NA18991.hp2 | 3_prime_UTR_variant | MODIFIER | c.*113G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 21/21 | 113 | chr4 | 140622082 | ||||||
chr4:140756096 | G | A | 2 | a0001c0001t0004 a0001c0001t0016 |
6 | NA18963.hp1 NA18991.hp2 NA19067.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-51C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/21 | 51 | chr4 | 140756096 | ||||||
chr4:140756171 | G | A | 8 | a0001c0001t0003 a0001c0001t0004 a0001c0001t0014 others(5): Show |
22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
5_prime_UTR_variant | MODIFIER | c.-126C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/21 | 126 | chr4 | 140756171 | ||||||
chr4:140756194 | G | A | 1 | a0001c0001t0017 | 1 | HG02258.hp2 | 5_prime_UTR_variant | MODIFIER | c.-149C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/21 | 149 | chr4 | 140756194 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:140623034 | C | A | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3079-117G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623034 | |||||||
chr4:140623124 | G | A | 3 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0178 |
3 | HG01106.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3079-207C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623124 | |||||||
chr4:140623230 | T | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.3079-313A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623230 | |||||||
chr4:140623259 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3079-342C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623259 | |||||||
chr4:140623265 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.3079-348G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623265 | |||||||
chr4:140623350 | G | A | 1 | a0001c0001t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3079-433C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623350 | |||||||
chr4:140623362 | C | T | 56 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(53): Show |
56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.3079-445G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623362 | |||||||
chr4:140623453 | C | T | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3079-536G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623453 | |||||||
chr4:140623455 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0250 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.3079-538T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623455 | |||||||
chr4:140623619 | C | T | 2 | a0001c0005t0002g0103 a0001c0005t0002g0104 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3078+497G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623619 | |||||||
chr4:140623837 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0060 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.3078+279C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623837 | |||||||
chr4:140623937 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0267 |
2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.3078+179G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140623937 | |||||||
chr4:140624007 | C | CAA | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.3078+108_3078+109i others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140624007 | |||||||
chr4:140624089 | C | G | 1 | a0001c0006t0007g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3078+27G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 20/20 | chr4 | 140624089 | |||||||
chr4:140624222 | A | G | 3 | a0001c0005t0001g0133 a0001c0005t0001g0146 a0001c0005t0001g0158 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
splice_region_variant&intron_variant | LOW | c.2975-3T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 19/20 | chr4 | 140624222 | |||||||
chr4:140624243 | A | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2975-24T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 19/20 | chr4 | 140624243 | |||||||
chr4:140624410 | G | GA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0035 others(32): Show |
35 | HG00733.hp2 HG00741.hp1 HG01175.hp1 others(32): Show |
intron_variant | MODIFIER | c.2900-23dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624410 | |||||||
chr4:140624445 | AT | A | 21 | a0001c0001t0002g0014 a0001c0001t0002g0044 a0001c0001t0002g0067 others(18): Show |
21 | HG00639.hp2 HG01074.hp1 HG01175.hp2 others(18): Show |
intron_variant | MODIFIER | c.2900-58delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624445 | |||||||
chr4:140624499 | GCAAA | G | 17 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0053 others(14): Show |
17 | HG00733.hp2 HG00741.hp1 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.2900-115_2900-112d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624499 | |||||||
chr4:140624512 | CA | C | 85 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2900-125delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624512 | |||||||
chr4:140624717 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0267 a0001c0004t0001g0273 |
3 | HG02451.hp1 HG02486.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2900-329C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624717 | |||||||
chr4:140624876 | A | T | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2900-488T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140624876 | |||||||
chr4:140625052 | CA | C | 121 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(118): Show |
121 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.2900-665delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625052 | |||||||
chr4:140625267 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2900-879T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625267 | |||||||
chr4:140625391 | C | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2900-1003G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625391 | |||||||
chr4:140625430 | G | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0052 others(4): Show |
7 | NA18948.hp2 NA18963.hp1 NA18967.hp1 others(4): Show |
intron_variant | MODIFIER | c.2900-1042C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625430 | |||||||
chr4:140625491 | C | T | 1 | a0001c0004t0005g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2900-1103G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625491 | |||||||
chr4:140625502 | C | T | 2 | a0001c0002t0001g0189 a0001c0002t0001g0200 |
2 | HG00099.hp2 HG00140.hp2 |
intron_variant | MODIFIER | c.2900-1114G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625502 | |||||||
chr4:140625937 | G | A | 2 | a0001c0003t0001g0194 a0001c0021t0001g0265 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2899+1504C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140625937 | |||||||
chr4:140626150 | G | A | 33 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0002g0044 others(30): Show |
33 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(30): Show |
intron_variant | MODIFIER | c.2899+1291C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626150 | |||||||
chr4:140626276 | A | G | 4 | a0001c0001t0002g0274 a0001c0005t0002g0128 a0001c0005t0002g0131 others(1): Show |
4 | HG00639.hp1 HG02300.hp1 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.2899+1165T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626276 | |||||||
chr4:140626282 | GC | G | 8 | a0001c0003t0001g0042 a0001c0003t0001g0056 a0001c0003t0001g0079 others(5): Show |
8 | HG00621.hp1 NA18943.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.2899+1158delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626282 | |||||||
chr4:140626293 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2899+1148G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626293 | |||||||
chr4:140626775 | C | T | 1 | a0001c0013t0011g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2899+666G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626775 | |||||||
chr4:140626843 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2899+598C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626843 | |||||||
chr4:140626927 | A | G | 3 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0178 |
3 | HG01106.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2899+514T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626927 | |||||||
chr4:140626958 | T | G | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2899+483A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140626958 | |||||||
chr4:140627059 | T | G | 3 | a0001c0001t0014g0284 a0001c0008t0005g0179 a0001c0008t0005g0242 |
3 | HG01261.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.2899+382A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140627059 | |||||||
chr4:140627415 | T | C | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2899+26A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 18/20 | chr4 | 140627415 | |||||||
chr4:140627769 | A | G | 248 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(245): Show |
248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.2813-242T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140627769 | |||||||
chr4:140627838 | G | T | 1 | a0001c0002t0001g0235 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.2813-311C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140627838 | |||||||
chr4:140627875 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2813-348G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140627875 | |||||||
chr4:140628016 | C | G | 4 | a0001c0001t0001g0238 a0001c0002t0001g0268 a0001c0002t0001g0269 others(1): Show |
4 | HG02896.hp1 HG02897.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.2812+284G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628016 | |||||||
chr4:140628199 | G | A | 1 | a0001c0004t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2812+101C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628199 | |||||||
chr4:140628239 | C | A | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2812+61G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628239 | |||||||
chr4:140628274 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2812+26T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 17/20 | chr4 | 140628274 | |||||||
chr4:140628660 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2747-295G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140628660 | |||||||
chr4:140628661 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.2747-296C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140628661 | |||||||
chr4:140628843 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2747-478T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140628843 | |||||||
chr4:140629021 | A | G | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2747-656T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629021 | |||||||
chr4:140629280 | G | A | 14 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(11): Show |
14 | HG01069.hp2 HG01192.hp1 HG02055.hp2 others(11): Show |
intron_variant | MODIFIER | c.2747-915C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629280 | |||||||
chr4:140629303 | G | A | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2747-938C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629303 | |||||||
chr4:140629378 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2747-1013A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629378 | |||||||
chr4:140629853 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2747-1488T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629853 | |||||||
chr4:140629925 | A | G | 5 | a0001c0003t0001g0031 a0001c0003t0001g0072 a0001c0003t0001g0074 others(2): Show |
5 | HG00558.hp1 HG00673.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2747-1560T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629925 | |||||||
chr4:140629977 | T | A | 1 | a0001c0001t0001g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2747-1612A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140629977 | |||||||
chr4:140630454 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2747-2089T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630454 | |||||||
chr4:140630496 | G | T | 56 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(53): Show |
56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2747-2131C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630496 | |||||||
chr4:140630533 | A | G | 1 | a0001c0002t0001g0215 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2747-2168T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630533 | |||||||
chr4:140630570 | G | A | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2747-2205C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630570 | |||||||
chr4:140630645 | G | A | 123 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(120): Show |
123 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.2747-2280C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630645 | |||||||
chr4:140630650 | G | A | 3 | a0001c0005t0001g0133 a0001c0005t0001g0146 a0001c0005t0001g0158 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2747-2285C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630650 | |||||||
chr4:140630779 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2747-2414T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630779 | |||||||
chr4:140630866 | T | C | 4 | a0001c0001t0001g0249 a0001c0002t0001g0065 a0001c0002t0001g0095 others(1): Show |
4 | NA18971.hp2 NA18975.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2747-2501A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140630866 | |||||||
chr4:140631060 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.2747-2695T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631060 | |||||||
chr4:140631335 | G | C | 4 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0172 others(1): Show |
4 | HG02622.hp2 HG02723.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2746+2613C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631335 | |||||||
chr4:140631367 | C | A | 1 | a0001c0006t0001g0258 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.2746+2581G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631367 | |||||||
chr4:140631383 | C | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2746+2565G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631383 | |||||||
chr4:140631423 | G | A | 1 | a0001c0005t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2746+2525C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631423 | |||||||
chr4:140631434 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2746+2514C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631434 | |||||||
chr4:140631448 | C | T | 29 | a0001c0001t0001g0004 a0001c0001t0001g0032 a0001c0001t0001g0035 others(26): Show |
29 | HG00733.hp2 HG00741.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.2746+2500G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631448 | |||||||
chr4:140631601 | CT | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(204): Show |
207 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.2746+2346delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631601 | |||||||
chr4:140631667 | G | A | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2746+2281C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631667 | |||||||
chr4:140631823 | C | T | 56 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(53): Show |
56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2746+2125G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631823 | |||||||
chr4:140631950 | C | T | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2746+1998G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631950 | |||||||
chr4:140631998 | A | G | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2746+1950T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140631998 | |||||||
chr4:140632087 | C | T | 3 | a0001c0005t0001g0133 a0001c0005t0001g0146 a0001c0005t0001g0158 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2746+1861G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632087 | |||||||
chr4:140632217 | A | G | 6 | a0001c0001t0001g0016 a0001c0001t0001g0027 a0001c0001t0001g0052 others(3): Show |
6 | NA18948.hp2 NA18963.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.2746+1731T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632217 | |||||||
chr4:140632262 | G | GT | 164 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(161): Show |
164 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2746+1685dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632262 | |||||||
chr4:140632262 | G | GTT | 58 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(55): Show |
58 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.2746+1684_2746+168 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632262 | |||||||
chr4:140632262 | G | GTTTT | 25 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0066 others(22): Show |
25 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.2746+1682_2746+168 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632262 | |||||||
chr4:140632266 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2746+1682A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632266 | |||||||
chr4:140632302 | T | C | 1 | a0001c0001t0002g0044 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2746+1646A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632302 | |||||||
chr4:140632346 | G | A | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2746+1602C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632346 | |||||||
chr4:140632637 | G | A | 25 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0066 others(22): Show |
25 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(22): Show |
intron_variant | MODIFIER | c.2746+1311C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632637 | |||||||
chr4:140632710 | G | A | 1 | a0001c0005t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2746+1238C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632710 | |||||||
chr4:140632861 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2746+1087G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632861 | |||||||
chr4:140632882 | G | A | 1 | a0001c0003t0001g0074 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2746+1066C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632882 | |||||||
chr4:140632991 | A | G | 85 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(82): Show |
85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.2746+957T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140632991 | |||||||
chr4:140633115 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2746+833G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633115 | |||||||
chr4:140633265 | C | T | 1 | a0001c0005t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2746+683G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633265 | |||||||
chr4:140633418 | G | A | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2746+530C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633418 | |||||||
chr4:140633463 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0045 a0001c0001t0001g0073 others(2): Show |
5 | HG00408.hp1 HG00609.hp1 HG00621.hp2 others(2): Show |
intron_variant | MODIFIER | c.2746+485G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633463 | |||||||
chr4:140633612 | A | G | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2746+336T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633612 | |||||||
chr4:140633795 | G | A | 122 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(119): Show |
122 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.2746+153C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633795 | |||||||
chr4:140633908 | G | T | 211 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(208): Show |
211 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(208): Show |
intron_variant | MODIFIER | c.2746+40C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 16/20 | chr4 | 140633908 | |||||||
chr4:140634301 | G | C | 5 | a0001c0001t0001g0094 a0001c0001t0001g0155 a0001c0002t0001g0196 others(2): Show |
5 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2506-113C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634301 | |||||||
chr4:140634361 | A | T | 84 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0026 others(81): Show |
84 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.2506-173T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634361 | |||||||
chr4:140634496 | C | T | 1 | a0001c0001t0001g0110 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.2506-308G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634496 | |||||||
chr4:140634497 | A | G | 291 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(288): Show |
292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.2506-309T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634497 | |||||||
chr4:140634571 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2506-383A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634571 | |||||||
chr4:140634592 | C | T | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2506-404G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634592 | |||||||
chr4:140634749 | A | G | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2506-561T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634749 | |||||||
chr4:140634785 | A | G | 1 | a0001c0002t0001g0214 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.2506-597T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634785 | |||||||
chr4:140634973 | T | C | 2 | a0001c0003t0001g0194 a0001c0021t0001g0265 |
2 | HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2506-785A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140634973 | |||||||
chr4:140635179 | G | GA | 8 | a0001c0001t0001g0053 a0001c0001t0001g0054 a0001c0001t0002g0044 others(5): Show |
8 | HG00741.hp1 HG01256.hp2 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2506-992dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635179 | |||||||
chr4:140635180 | A | G | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2506-992T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635180 | |||||||
chr4:140635248 | C | T | 23 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(20): Show |
23 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2506-1060G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635248 | |||||||
chr4:140635258 | G | A | 56 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(53): Show |
56 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.2506-1070C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635258 | |||||||
chr4:140635315 | GA | G | 86 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(83): Show |
86 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.2506-1128delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635315 | |||||||
chr4:140635384 | A | C | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2506-1196T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635384 | |||||||
chr4:140635393 | G | A | 59 | a0001c0001t0001g0003 a0001c0001t0001g0144 a0001c0001t0001g0145 others(56): Show |
59 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(56): Show |
intron_variant | MODIFIER | c.2506-1205C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635393 | |||||||
chr4:140635636 | T | C | 181 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(178): Show |
181 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.2506-1448A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635636 | |||||||
chr4:140635721 | G | A | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2506-1533C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140635721 | |||||||
chr4:140636338 | A | G | 6 | a0001c0001t0001g0094 a0001c0001t0001g0141 a0001c0001t0001g0155 others(3): Show |
6 | HG01243.hp1 HG01496.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2506-2150T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636338 | |||||||
chr4:140636534 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2506-2346A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636534 | |||||||
chr4:140636606 | A | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2506-2418T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636606 | |||||||
chr4:140636787 | T | C | 8 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0002t0001g0101 others(5): Show |
8 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.2505+2299A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636787 | |||||||
chr4:140636880 | C | T | 1 | a0001c0001t0001g0045 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2505+2206G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636880 | |||||||
chr4:140636956 | G | C | 1 | a0001c0003t0001g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2505+2130C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636956 | |||||||
chr4:140636969 | C | G | 87 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(84): Show |
87 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(84): Show |
intron_variant | MODIFIER | c.2505+2117G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140636969 | |||||||
chr4:140637022 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0178 |
2 | HG01106.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2505+2064C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637022 | |||||||
chr4:140637070 | A | G | 1 | a0001c0012t0008g0147 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2505+2016T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637070 | |||||||
chr4:140637121 | G | A | 1 | a0001c0004t0001g0120 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2505+1965C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637121 | |||||||
chr4:140637136 | G | A | 15 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(12): Show |
15 | HG01069.hp2 HG01192.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2505+1950C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637136 | |||||||
chr4:140637148 | G | A | 3 | a0001c0005t0001g0133 a0001c0005t0001g0146 a0001c0005t0001g0158 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2505+1938C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637148 | |||||||
chr4:140637148 | G | C | 1 | a0001c0001t0001g0204 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.2505+1938C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637148 | |||||||
chr4:140637187 | T | C | 1 | a0001c0004t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2505+1899A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637187 | |||||||
chr4:140637200 | A | G | 23 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(20): Show |
23 | HG00735.hp1 HG01069.hp2 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2505+1886T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637200 | |||||||
chr4:140637265 | G | A | 2 | a0001c0002t0001g0201 a0001c0004t0001g0143 |
2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2505+1821C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637265 | |||||||
chr4:140637357 | G | GA | 74 | a0001c0001t0001g0008 a0001c0001t0001g0144 a0001c0001t0001g0145 others(71): Show |
74 | HG00140.hp1 HG00621.hp1 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.2505+1728dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637357 | |||||||
chr4:140637420 | T | C | 88 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(85): Show |
88 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.2505+1666A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637420 | |||||||
chr4:140637463 | C | T | 1 | a0001c0001t0001g0154 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2505+1623G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637463 | |||||||
chr4:140637540 | C | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(24): Show |
27 | HG00408.hp2 HG01891.hp1 HG02056.hp2 others(24): Show |
intron_variant | MODIFIER | c.2505+1546G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637540 | |||||||
chr4:140637708 | T | A | 3 | a0001c0005t0001g0133 a0001c0005t0001g0146 a0001c0005t0001g0158 |
3 | HG02895.hp2 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2505+1378A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637708 | |||||||
chr4:140637872 | G | A | 23 | a0001c0001t0001g0008 a0001c0001t0001g0028 a0001c0001t0001g0029 others(20): Show |
23 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.2505+1214C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637872 | |||||||
chr4:140637997 | A | G | 2 | a0001c0001t0001g0070 a0001c0004t0001g0114 |
2 | NA20300.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2505+1089T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140637997 | |||||||
chr4:140638022 | A | G | 1 | a0001c0003t0001g0038 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.2505+1064T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638022 | |||||||
chr4:140638439 | C | T | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2505+647G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638439 | |||||||
chr4:140638459 | C | G | 1 | a0001c0004t0001g0120 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2505+627G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638459 | |||||||
chr4:140638535 | A | G | 2 | a0001c0001t0001g0045 a0001c0001t0001g0083 |
2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.2505+551T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638535 | |||||||
chr4:140638612 | G | A | 1 | a0001c0002t0001g0231 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.2505+474C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 15/20 | chr4 | 140638612 | |||||||
chr4:140639446 | T | C | 1 | a0001c0001t0004g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.2338-18A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639446 | |||||||
chr4:140639583 | C | CCA | 34 | a0001c0001t0002g0014 a0001c0001t0002g0039 a0001c0001t0002g0044 others(31): Show |
34 | HG00140.hp1 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.2338-157_2338-156d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639583 | |||||||
chr4:140639634 | C | T | 247 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(244): Show |
247 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.2338-206G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639634 | |||||||
chr4:140639704 | C | T | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2338-276G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639704 | |||||||
chr4:140639815 | T | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
213 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.2338-387A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639815 | |||||||
chr4:140639875 | C | T | 3 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0178 |
3 | HG01106.hp2 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2338-447G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639875 | |||||||
chr4:140639899 | C | T | 2 | a0001c0001t0002g0157 a0001c0001t0002g0250 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2338-471G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639899 | |||||||
chr4:140639996 | T | C | 4 | a0001c0001t0001g0024 a0001c0001t0003g0278 a0001c0001t0003g0279 others(1): Show |
4 | HG01081.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.2338-568A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140639996 | |||||||
chr4:140640086 | A | G | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2338-658T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640086 | |||||||
chr4:140640199 | G | T | 88 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(85): Show |
88 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(85): Show |
intron_variant | MODIFIER | c.2338-771C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640199 | |||||||
chr4:140640300 | A | G | 91 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(88): Show |
91 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.2338-872T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640300 | |||||||
chr4:140640403 | G | A | 116 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(113): Show |
116 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(113): Show |
intron_variant | MODIFIER | c.2338-975C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640403 | |||||||
chr4:140640447 | TG | T | 216 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(213): Show |
216 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.2338-1020delC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640447 | |||||||
chr4:140640450 | G | C | 5 | a0001c0001t0001g0141 a0001c0001t0001g0155 a0001c0002t0001g0196 others(2): Show |
5 | HG01243.hp1 HG01496.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-1022C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640450 | |||||||
chr4:140640560 | G | T | 25 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(22): Show |
25 | HG00408.hp2 HG01106.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.2338-1132C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640560 | |||||||
chr4:140640684 | C | T | 93 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(90): Show |
93 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.2338-1256G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640684 | |||||||
chr4:140640743 | A | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(90): Show |
93 | HG00140.hp1 HG00408.hp2 HG00558.hp1 others(90): Show |
intron_variant | MODIFIER | c.2338-1315T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640743 | |||||||
chr4:140640743 | A | T | 5 | a0001c0001t0005g0096 a0001c0001t0014g0284 a0001c0004t0005g0266 others(2): Show |
5 | HG01261.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-1315T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640743 | |||||||
chr4:140640785 | T | C | 2 | a0001c0001t0002g0157 a0001c0001t0002g0250 |
2 | HG02055.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.2338-1357A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640785 | |||||||
chr4:140640795 | C | T | 24 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(21): Show |
24 | HG00408.hp2 HG01106.hp2 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.2338-1367G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640795 | |||||||
chr4:140640833 | C | CATTCTTA others(2): Show |
40 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(37): Show |
40 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.2338-1406_2338-140 others(13): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640833 | |||||||
chr4:140640868 | C | T | 2 | a0001c0003t0001g0072 a0001c0003t0001g0074 |
2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.2338-1440G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640868 | |||||||
chr4:140640876 | C | CATATATA others(13): Show |
25 | a0001c0001t0001g0003 a0001c0001t0001g0093 a0001c0001t0002g0270 others(22): Show |
25 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.2338-1449_2338-144 others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640876 | |||||||
chr4:140640876 | C | CATATATA others(13): Show |
15 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(12): Show |
15 | HG00408.hp2 HG02056.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2338-1449_2338-144 others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640876 | |||||||
chr4:140640890 | CTA | C | 15 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0026 others(12): Show |
15 | HG00408.hp2 HG02056.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.2338-1464_2338-146 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640890 | |||||||
chr4:140640921 | G | A | 44 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0011 others(41): Show |
44 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(41): Show |
intron_variant | MODIFIER | c.2338-1493C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140640921 | |||||||
chr4:140641090 | C | CA | 6 | a0001c0001t0001g0139 a0001c0001t0001g0178 a0001c0001t0001g0267 others(3): Show |
6 | HG01106.hp2 HG01361.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.2338-1663dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641090 | C | CAA | 8 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0006g0142 others(5): Show |
8 | HG01069.hp2 HG01192.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.2338-1664_2338-166 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641090 | C | CAAA | 14 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 others(11): Show |
14 | HG00140.hp1 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.2338-1665_2338-166 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641090 | C | CAAAA | 22 | a0001c0001t0001g0028 a0001c0001t0001g0034 a0001c0001t0001g0036 others(19): Show |
22 | HG00558.hp2 HG00642.hp1 HG00733.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-1666_2338-166 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641090 | C | CAAAAA | 10 | a0001c0001t0001g0008 a0001c0001t0001g0029 a0001c0001t0001g0070 others(7): Show |
10 | HG01169.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2338-1667_2338-166 others(9): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641090 | C | CAAAAAAA others(3): Show |
3 | a0001c0004t0005g0266 a0001c0008t0005g0179 a0001c0016t0012g0272 |
3 | HG02559.hp1 HG02809.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2338-1672_2338-166 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641090 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2338-1675_2338-166 others(17): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641090 | |||||||
chr4:140641096 | AAAAAAAA others(2): Show |
A | 28 | a0001c0001t0001g0212 a0001c0001t0002g0014 a0001c0001t0002g0044 others(25): Show |
28 | HG00558.hp1 HG00639.hp1 HG00639.hp2 others(25): Show |
intron_variant | MODIFIER | c.2338-1677_2338-166 others(13): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641096 | |||||||
chr4:140641097 | AAAAAAAA others(1): Show |
A | 34 | a0001c0001t0001g0011 a0001c0001t0001g0026 a0001c0001t0001g0066 others(31): Show |
34 | HG00408.hp2 HG00735.hp1 HG01070.hp2 others(31): Show |
intron_variant | MODIFIER | c.2338-1677_2338-167 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641097 | |||||||
chr4:140641102 | AAAC | A | 64 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(61): Show |
64 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.2338-1677_2338-167 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641102 | |||||||
chr4:140641103 | AAC | A | 12 | a0001c0001t0001g0012 a0001c0001t0001g0021 a0001c0001t0001g0063 others(9): Show |
12 | HG00423.hp1 HG01243.hp2 HG01975.hp1 others(9): Show |
intron_variant | MODIFIER | c.2338-1677_2338-167 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641103 | |||||||
chr4:140641104 | AC | A | 43 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0032 others(40): Show |
43 | HG00544.hp2 HG00621.hp2 HG00733.hp2 others(40): Show |
intron_variant | MODIFIER | c.2338-1677delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641104 | |||||||
chr4:140641105 | C | A | 73 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0024 others(70): Show |
73 | HG00140.hp1 HG00558.hp2 HG00642.hp1 others(70): Show |
intron_variant | MODIFIER | c.2338-1677G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641105 | |||||||
chr4:140641162 | A | C | 5 | a0001c0001t0005g0096 a0001c0001t0014g0284 a0001c0004t0005g0266 others(2): Show |
5 | HG01261.hp2 HG02572.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-1734T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641162 | |||||||
chr4:140641282 | T | G | 1 | a0001c0002t0001g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2338-1854A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641282 | |||||||
chr4:140641339 | C | A | 2 | a0001c0001t0002g0270 a0001c0017t0001g0159 |
2 | HG02258.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.2338-1911G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641339 | |||||||
chr4:140641643 | G | A | 2 | a0001c0001t0001g0094 a0001c0001t0002g0183 |
2 | HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2338-2215C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641643 | |||||||
chr4:140641644 | G | T | 89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
90 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.2338-2216C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641644 | |||||||
chr4:140641656 | G | A | 16 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0271 others(13): Show |
16 | HG01070.hp2 HG01071.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2338-2228C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641656 | |||||||
chr4:140641739 | A | G | 2 | a0001c0002t0001g0181 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.2338-2311T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641739 | |||||||
chr4:140641831 | C | T | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2338-2403G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641831 | |||||||
chr4:140641858 | C | A | 55 | a0001c0001t0001g0006 a0001c0001t0001g0015 a0001c0001t0001g0020 others(52): Show |
55 | HG00544.hp1 HG00558.hp1 HG00639.hp2 others(52): Show |
intron_variant | MODIFIER | c.2338-2430G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641858 | |||||||
chr4:140641858 | C | G | 1 | a0001c0002t0001g0181 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2338-2430G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641858 | |||||||
chr4:140641950 | T | C | 1 | a0001c0004t0002g0261 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2338-2522A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641950 | |||||||
chr4:140641977 | G | T | 1 | a0001c0006t0001g0206 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2338-2549C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641977 | |||||||
chr4:140641984 | C | T | 6 | a0001c0001t0001g0035 a0001c0001t0001g0094 a0001c0001t0002g0183 others(3): Show |
6 | HG01255.hp2 HG02300.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2338-2556G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140641984 | |||||||
chr4:140642027 | A | G | 1 | a0001c0007t0001g0230 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2338-2599T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642027 | |||||||
chr4:140642454 | T | C | 1 | a0001c0003t0001g0025 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2338-3026A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642454 | |||||||
chr4:140642484 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2338-3056A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642484 | |||||||
chr4:140642490 | C | G | 3 | a0001c0005t0002g0128 a0001c0005t0002g0131 a0001c0008t0002g0187 |
3 | HG00639.hp1 HG02300.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2338-3062G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642490 | |||||||
chr4:140642593 | A | G | 43 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(40): Show |
43 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2338-3165T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642593 | |||||||
chr4:140642691 | A | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-3263T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642691 | |||||||
chr4:140642806 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2338-3378A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642806 | |||||||
chr4:140642838 | T | G | 255 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(252): Show |
255 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(252): Show |
intron_variant | MODIFIER | c.2338-3410A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642838 | |||||||
chr4:140642842 | G | A | 2 | a0001c0005t0001g0132 a0001c0005t0001g0133 |
2 | HG02630.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.2338-3414C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642842 | |||||||
chr4:140642846 | G | A | 1 | a0001c0002t0001g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.2338-3418C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642846 | |||||||
chr4:140642861 | C | A | 1 | a0001c0004t0001g0173 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2338-3433G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140642861 | |||||||
chr4:140643072 | A | G | 3 | a0001c0005t0002g0128 a0001c0005t0002g0131 a0001c0008t0002g0187 |
3 | HG00639.hp1 HG02300.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.2338-3644T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643072 | |||||||
chr4:140643388 | C | T | 12 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0002t0001g0101 others(9): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2338-3960G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643388 | |||||||
chr4:140643402 | C | CCAGGGTG others(2): Show |
251 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2338-3975_2338-397 others(13): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643402 | |||||||
chr4:140643431 | G | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0177 others(4): Show |
7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2338-4003C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643431 | |||||||
chr4:140643556 | T | C | 2 | a0001c0001t0001g0139 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4128A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643556 | |||||||
chr4:140643578 | A | G | 251 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(248): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.2338-4150T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643578 | |||||||
chr4:140643636 | G | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-4208C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643636 | |||||||
chr4:140643742 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0182 |
3 | HG03704.hp1 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.2338-4314C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643742 | |||||||
chr4:140643771 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4343C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140643771 | |||||||
chr4:140644122 | C | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(39): Show |
42 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2338-4694G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644122 | |||||||
chr4:140644194 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4766C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644194 | |||||||
chr4:140644338 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-4910C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644338 | |||||||
chr4:140644420 | G | T | 45 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0073 others(42): Show |
45 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(42): Show |
intron_variant | MODIFIER | c.2338-4992C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644420 | |||||||
chr4:140644437 | C | T | 2 | a0001c0001t0001g0139 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-5009G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644437 | |||||||
chr4:140644440 | G | A | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-5012C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644440 | |||||||
chr4:140644556 | C | T | 42 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(39): Show |
42 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2338-5128G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644556 | |||||||
chr4:140644612 | G | A | 20 | a0001c0001t0001g0162 a0001c0001t0001g0267 a0001c0001t0002g0090 others(17): Show |
20 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(17): Show |
intron_variant | MODIFIER | c.2338-5184C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644612 | |||||||
chr4:140644712 | C | G | 66 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0036 others(63): Show |
66 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.2338-5284G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644712 | |||||||
chr4:140644716 | G | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0177 others(4): Show |
7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.2338-5288C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644716 | |||||||
chr4:140644801 | G | A | 2 | a0001c0001t0001g0139 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.2338-5373C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644801 | |||||||
chr4:140644815 | G | A | 3 | a0001c0001t0001g0267 a0001c0001t0014g0284 a0001c0004t0005g0266 |
3 | HG02451.hp1 HG02723.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2338-5387C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644815 | |||||||
chr4:140644859 | C | T | 1 | a0001c0002t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2338-5431G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644859 | |||||||
chr4:140644951 | A | G | 10 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0177 others(7): Show |
10 | HG01106.hp2 HG02055.hp2 HG02165.hp2 others(7): Show |
intron_variant | MODIFIER | c.2338-5523T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644951 | |||||||
chr4:140644964 | C | T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
195 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.2338-5536G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644964 | |||||||
chr4:140644975 | G | A | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2338-5547C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140644975 | |||||||
chr4:140645017 | G | T | 1 | a0001c0004t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2338-5589C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645017 | |||||||
chr4:140645021 | G | A | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.2338-5593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645021 | |||||||
chr4:140645037 | C | T | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-5609G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645037 | |||||||
chr4:140645058 | C | G | 1 | a0001c0004t0001g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.2338-5630G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645058 | |||||||
chr4:140645235 | G | A | 6 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0094 others(3): Show |
6 | HG02280.hp1 HG02280.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.2338-5807C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645235 | |||||||
chr4:140645458 | C | T | 1 | a0001c0003t0001g0084 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.2338-6030G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645458 | |||||||
chr4:140645459 | G | C | 42 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(39): Show |
42 | HG00099.hp2 HG00140.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2338-6031C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645459 | |||||||
chr4:140645544 | G | A | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2338-6116C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645544 | |||||||
chr4:140645701 | C | G | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.2338-6273G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645701 | |||||||
chr4:140645730 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(84): Show |
87 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.2338-6302G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645730 | |||||||
chr4:140645926 | C | T | 1 | a0001c0003t0007g0013 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2338-6498G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140645926 | |||||||
chr4:140646130 | G | A | 8 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0271 others(5): Show |
8 | HG01261.hp2 HG02258.hp2 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.2338-6702C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646130 | |||||||
chr4:140646201 | G | T | 1 | a0001c0002t0002g0232 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.2338-6773C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646201 | |||||||
chr4:140646318 | C | T | 1 | a0001c0004t0001g0120 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.2338-6890G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646318 | |||||||
chr4:140646373 | C | A | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2338-6945G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646373 | |||||||
chr4:140646478 | A | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2338-7050T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646478 | |||||||
chr4:140646514 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2338-7086A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646514 | |||||||
chr4:140646527 | T | C | 1 | a0001c0002t0001g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.2338-7099A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646527 | |||||||
chr4:140646847 | G | A | 4 | a0001c0001t0001g0034 a0001c0001t0001g0059 a0001c0001t0001g0061 others(1): Show |
4 | HG03704.hp1 HG03710.hp1 HG03710.hp2 others(1): Show |
intron_variant | MODIFIER | c.2338-7419C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646847 | |||||||
chr4:140646851 | C | T | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2338-7423G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140646851 | |||||||
chr4:140647067 | A | G | 1 | a0001c0001t0001g0139 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2338-7639T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647067 | |||||||
chr4:140647193 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2338-7765G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647193 | |||||||
chr4:140647466 | A | T | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2338-8038T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647466 | |||||||
chr4:140647505 | C | A | 1 | a0003c0019t0002g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2338-8077G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647505 | |||||||
chr4:140647658 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(105): Show |
108 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.2338-8230G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647658 | |||||||
chr4:140647666 | G | A | 2 | a0001c0002t0001g0197 a0001c0002t0001g0198 |
2 | HG01081.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2338-8238C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647666 | |||||||
chr4:140647791 | T | C | 1 | a0001c0002t0001g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2338-8363A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647791 | |||||||
chr4:140647824 | C | T | 1 | a0001c0013t0011g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2338-8396G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647824 | |||||||
chr4:140647856 | G | A | 3 | a0001c0001t0001g0145 a0001c0001t0001g0149 a0001c0001t0001g0151 |
3 | HG01884.hp2 HG02970.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2338-8428C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647856 | |||||||
chr4:140647894 | TGGGGGTC others(21): Show |
T | 5 | a0001c0001t0001g0073 a0001c0003t0001g0072 a0001c0003t0001g0074 others(2): Show |
5 | HG00408.hp1 HG00673.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2338-8494_2338-846 others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140647894 | |||||||
chr4:140648231 | T | C | 11 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0271 others(8): Show |
11 | HG01261.hp2 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2338-8803A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648231 | |||||||
chr4:140648236 | G | T | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2338-8808C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648236 | |||||||
chr4:140648385 | G | GT | 12 | a0001c0001t0001g0162 a0001c0001t0001g0164 a0001c0001t0001g0251 others(9): Show |
12 | HG00642.hp2 HG00741.hp1 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.2337+8711dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648385 | |||||||
chr4:140648385 | G | GTT | 13 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0002t0001g0101 others(10): Show |
13 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(10): Show |
intron_variant | MODIFIER | c.2337+8710_2337+871 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648385 | |||||||
chr4:140648385 | G | T | 1 | a0001c0001t0002g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2337+8712C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648385 | |||||||
chr4:140648387 | T | TG | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+8709_2337+871 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648387 | |||||||
chr4:140648388 | T | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2337+8709A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648388 | |||||||
chr4:140648542 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0094 others(2): Show |
5 | HG02280.hp1 HG02717.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+8555G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648542 | |||||||
chr4:140648567 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0271 others(4): Show |
7 | HG02258.hp2 HG02717.hp1 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2337+8530C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648567 | |||||||
chr4:140648630 | C | T | 6 | a0001c0001t0001g0006 a0001c0001t0001g0060 a0001c0001t0001g0123 others(3): Show |
6 | HG01496.hp2 HG01515.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.2337+8467G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648630 | |||||||
chr4:140648693 | C | T | 52 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(49): Show |
52 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.2337+8404G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648693 | |||||||
chr4:140648909 | GC | G | 67 | a0001c0001t0001g0003 a0001c0001t0001g0011 a0001c0001t0001g0036 others(64): Show |
67 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(64): Show |
intron_variant | MODIFIER | c.2337+8187delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648909 | |||||||
chr4:140648977 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+8120A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140648977 | |||||||
chr4:140649165 | C | T | 88 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(85): Show |
88 | HG00423.hp1 HG00423.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.2337+7932G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649165 | |||||||
chr4:140649167 | G | A | 11 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0271 others(8): Show |
11 | HG01261.hp2 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2337+7930C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649167 | |||||||
chr4:140649276 | T | C | 1 | a0001c0010t0001g0191 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2337+7821A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649276 | |||||||
chr4:140649368 | G | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0177 others(5): Show |
8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+7729C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649368 | |||||||
chr4:140649518 | A | G | 253 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2337+7579T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649518 | |||||||
chr4:140649540 | C | A | 2 | a0001c0001t0004g0293 a0001c0001t0016g0295 |
2 | NA18991.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.2337+7557G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649540 | |||||||
chr4:140649549 | T | C | 3 | a0001c0001t0001g0204 a0001c0001t0001g0218 a0001c0002t0001g0065 |
3 | HG02523.hp2 NA18941.hp2 NA18971.hp2 |
intron_variant | MODIFIER | c.2337+7548A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649549 | |||||||
chr4:140649552 | A | T | 22 | a0001c0001t0001g0162 a0001c0001t0001g0267 a0001c0001t0002g0090 others(19): Show |
22 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(19): Show |
intron_variant | MODIFIER | c.2337+7545T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649552 | |||||||
chr4:140649563 | A | T | 49 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(46): Show |
49 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.2337+7534T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649563 | |||||||
chr4:140649630 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.2337+7467G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649630 | |||||||
chr4:140649659 | G | A | 33 | a0001c0001t0001g0036 a0001c0001t0001g0073 a0001c0001t0002g0039 others(30): Show |
33 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.2337+7438C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649659 | |||||||
chr4:140649743 | C | A | 139 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
139 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.2337+7354G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649743 | |||||||
chr4:140649823 | A | G | 1 | a0001c0005t0001g0133 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2337+7274T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649823 | |||||||
chr4:140649868 | C | T | 7 | a0001c0001t0001g0168 a0001c0002t0001g0051 a0001c0002t0001g0189 others(4): Show |
7 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(4): Show |
intron_variant | MODIFIER | c.2337+7229G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140649868 | |||||||
chr4:140650042 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2337+7055T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650042 | |||||||
chr4:140650060 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2337+7037A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650060 | |||||||
chr4:140650603 | G | C | 1 | a0001c0001t0001g0008 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2337+6494C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650603 | |||||||
chr4:140650746 | G | A | 46 | a0001c0001t0001g0011 a0001c0001t0001g0036 a0001c0001t0001g0073 others(43): Show |
46 | HG00140.hp1 HG00408.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.2337+6351C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650746 | |||||||
chr4:140650911 | T | C | 1 | a0001c0004t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.2337+6186A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140650911 | |||||||
chr4:140651522 | G | A | 6 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0002t0001g0101 others(3): Show |
6 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.2337+5575C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651522 | |||||||
chr4:140651522 | GGGTGA | G | 22 | a0001c0001t0001g0007 a0001c0001t0001g0016 a0001c0001t0001g0024 others(19): Show |
22 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(19): Show |
intron_variant | MODIFIER | c.2337+5570_2337+557 others(9): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651522 | |||||||
chr4:140651600 | G | A | 1 | a0001c0003t0001g0022 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2337+5497C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651600 | |||||||
chr4:140651628 | G | A | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+5469C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651628 | |||||||
chr4:140651639 | T | C | 5 | a0001c0001t0001g0012 a0001c0002t0001g0224 a0001c0006t0001g0030 others(2): Show |
5 | HG00423.hp1 NA18948.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+5458A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651639 | |||||||
chr4:140651860 | G | A | 1 | a0001c0002t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2337+5237C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651860 | |||||||
chr4:140651976 | A | T | 253 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.2337+5121T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140651976 | |||||||
chr4:140652159 | T | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0135 a0001c0001t0001g0141 others(16): Show |
19 | HG01106.hp2 HG01261.hp2 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.2337+4938A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652159 | |||||||
chr4:140652195 | C | T | 5 | a0001c0001t0001g0012 a0001c0002t0001g0224 a0001c0006t0001g0030 others(2): Show |
5 | HG00423.hp1 NA18948.hp1 NA18979.hp2 others(2): Show |
intron_variant | MODIFIER | c.2337+4902G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652195 | |||||||
chr4:140652244 | T | TA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0164 others(5): Show |
8 | HG01106.hp2 HG01192.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.2337+4852dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652244 | |||||||
chr4:140652244 | TA | T | 14 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0091 others(11): Show |
14 | HG01169.hp1 HG01257.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.2337+4852delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652244 | |||||||
chr4:140652412 | A | G | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0001t0002g0183 |
3 | HG02717.hp2 HG02809.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.2337+4685T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652412 | |||||||
chr4:140652586 | G | T | 12 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0002t0001g0101 others(9): Show |
12 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.2337+4511C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652586 | |||||||
chr4:140652588 | A | G | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2337+4509T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652588 | |||||||
chr4:140652919 | C | T | 1 | a0001c0001t0004g0294 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2337+4178G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652919 | |||||||
chr4:140652951 | C | T | 1 | a0001c0001t0001g0063 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2337+4146G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140652951 | |||||||
chr4:140653004 | G | C | 118 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(115): Show |
118 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.2337+4093C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653004 | |||||||
chr4:140653069 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2337+4028G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653069 | |||||||
chr4:140653086 | G | A | 43 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(40): Show |
43 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(40): Show |
intron_variant | MODIFIER | c.2337+4011C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653086 | |||||||
chr4:140653160 | ATGAG | A | 11 | a0001c0001t0001g0135 a0001c0001t0001g0141 a0001c0001t0001g0271 others(8): Show |
11 | HG01261.hp2 HG02165.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.2337+3933_2337+393 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653160 | |||||||
chr4:140653229 | C | T | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2337+3868G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653229 | |||||||
chr4:140653265 | T | G | 13 | a0001c0001t0001g0011 a0001c0001t0001g0167 a0001c0001t0001g0199 others(10): Show |
13 | HG01074.hp2 HG01243.hp1 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.2337+3832A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653265 | |||||||
chr4:140653269 | T | C | 138 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(135): Show |
138 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.2337+3828A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653269 | |||||||
chr4:140653389 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2337+3708G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653389 | |||||||
chr4:140653459 | G | A | 107 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0011 others(104): Show |
107 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(104): Show |
intron_variant | MODIFIER | c.2337+3638C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653459 | |||||||
chr4:140653514 | T | C | 14 | a0001c0001t0001g0162 a0001c0001t0002g0270 a0001c0001t0003g0287 others(11): Show |
14 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.2337+3583A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653514 | |||||||
chr4:140653660 | G | T | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2337+3437C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653660 | |||||||
chr4:140653895 | C | T | 1 | a0001c0001t0001g0020 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2337+3202G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140653895 | |||||||
chr4:140654168 | G | A | 1 | a0001c0003t0001g0025 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2337+2929C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654168 | |||||||
chr4:140654192 | T | C | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+2905A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654192 | |||||||
chr4:140654241 | C | T | 4 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(1): Show |
4 | HG01243.hp2 HG01358.hp2 HG01928.hp1 others(1): Show |
intron_variant | MODIFIER | c.2337+2856G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654241 | |||||||
chr4:140654397 | T | C | 3 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0004t0001g0087 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2337+2700A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654397 | |||||||
chr4:140654441 | A | C | 262 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): Show |
intron_variant | MODIFIER | c.2337+2656T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654441 | |||||||
chr4:140654448 | A | G | 3 | a0001c0002t0001g0268 a0001c0002t0001g0269 a0001c0004t0001g0087 |
3 | HG02896.hp1 HG02897.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.2337+2649T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654448 | |||||||
chr4:140654474 | T | TG | 85 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0011 others(82): Show |
85 | HG00423.hp2 HG00544.hp1 HG00558.hp1 others(82): Show |
intron_variant | MODIFIER | c.2337+2622dupC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654474 | |||||||
chr4:140654474 | TG | T | 55 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(52): Show |
55 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(52): Show |
intron_variant | MODIFIER | c.2337+2622delC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654474 | |||||||
chr4:140654487 | T | C | 47 | a0001c0001t0001g0010 a0001c0001t0001g0028 a0001c0001t0001g0029 others(44): Show |
47 | HG00099.hp1 HG00544.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.2337+2610A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654487 | |||||||
chr4:140654718 | C | T | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2337+2379G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654718 | |||||||
chr4:140654836 | A | T | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.2337+2261T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654836 | |||||||
chr4:140654900 | C | T | 7 | a0001c0001t0001g0141 a0001c0001t0017g0297 a0001c0002t0001g0245 others(4): Show |
7 | HG01261.hp2 HG02258.hp2 HG03486.hp2 others(4): Show |
intron_variant | MODIFIER | c.2337+2197G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654900 | |||||||
chr4:140654941 | A | G | 1 | a0001c0001t0003g0289 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2337+2156T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654941 | |||||||
chr4:140654996 | T | C | 1 | a0001c0002t0001g0263 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2337+2101A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140654996 | |||||||
chr4:140655368 | AT | A | 33 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(30): Show |
33 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(30): Show |
intron_variant | MODIFIER | c.2337+1728delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655368 | |||||||
chr4:140655425 | A | T | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2337+1672T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655425 | |||||||
chr4:140655519 | G | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(87): Show |
90 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(87): Show |
intron_variant | MODIFIER | c.2337+1578C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655519 | |||||||
chr4:140655521 | T | G | 2 | a0001c0002t0001g0210 a0001c0002t0001g0223 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.2337+1576A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655521 | |||||||
chr4:140655530 | T | C | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.2337+1567A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655530 | |||||||
chr4:140655605 | T | C | 2 | a0001c0001t0001g0164 a0001c0004t0001g0273 |
2 | HG01192.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.2337+1492A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655605 | |||||||
chr4:140655675 | C | T | 2 | a0001c0005t0001g0160 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2337+1422G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655675 | |||||||
chr4:140655750 | A | G | 20 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(17): Show |
20 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.2337+1347T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655750 | |||||||
chr4:140655955 | A | T | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2337+1142T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140655955 | |||||||
chr4:140656081 | A | G | 1 | a0001c0003t0007g0013 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2337+1016T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656081 | |||||||
chr4:140656181 | T | G | 1 | a0001c0008t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2337+916A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656181 | |||||||
chr4:140656209 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2337+888G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656209 | |||||||
chr4:140656371 | T | C | 1 | a0001c0003t0001g0022 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2337+726A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656371 | |||||||
chr4:140656529 | A | G | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2337+568T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656529 | |||||||
chr4:140656622 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2337+475A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656622 | |||||||
chr4:140656781 | A | G | 2 | a0001c0004t0005g0266 a0001c0013t0011g0116 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2337+316T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656781 | |||||||
chr4:140656812 | C | T | 2 | a0001c0001t0001g0167 a0001c0002t0003g0283 |
2 | HG01255.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2337+285G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656812 | |||||||
chr4:140656817 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2337+280T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656817 | |||||||
chr4:140656881 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2337+216C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656881 | |||||||
chr4:140656933 | A | C | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.2337+164T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656933 | |||||||
chr4:140656958 | G | A | 31 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(28): Show |
31 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.2337+139C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140656958 | |||||||
chr4:140657001 | C | T | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.2337+96G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 13/20 | chr4 | 140657001 | |||||||
chr4:140657492 | G | A | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.2207+35C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 12/20 | chr4 | 140657492 | |||||||
chr4:140657957 | G | A | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1922-145C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140657957 | |||||||
chr4:140657993 | C | T | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1922-181G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140657993 | |||||||
chr4:140658035 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1922-223T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658035 | |||||||
chr4:140658054 | A | G | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1922-242T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658054 | |||||||
chr4:140658097 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1922-285C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658097 | |||||||
chr4:140658220 | G | A | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1922-408C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658220 | |||||||
chr4:140658247 | A | C | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1922-435T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658247 | |||||||
chr4:140658288 | A | G | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1922-476T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658288 | |||||||
chr4:140658300 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1922-488G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658300 | |||||||
chr4:140658503 | C | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(189): Show |
192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.1922-691G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658503 | |||||||
chr4:140658541 | A | T | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1922-729T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658541 | |||||||
chr4:140658547 | T | A | 40 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0016 others(37): Show |
40 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.1922-735A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658547 | |||||||
chr4:140658571 | A | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.1922-759T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658571 | |||||||
chr4:140658584 | C | T | 35 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0033 others(32): Show |
35 | HG00099.hp1 HG00544.hp2 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.1922-772G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658584 | |||||||
chr4:140658681 | G | T | 188 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(185): Show |
188 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1922-869C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658681 | |||||||
chr4:140658743 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1921+845C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658743 | |||||||
chr4:140658767 | C | G | 2 | a0001c0004t0001g0111 a0001c0005t0001g0129 |
2 | HG02622.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.1921+821G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658767 | |||||||
chr4:140658808 | TA | T | 9 | a0001c0001t0001g0080 a0001c0003t0001g0042 a0001c0003t0001g0043 others(6): Show |
9 | HG00621.hp1 HG02723.hp2 HG03453.hp2 others(6): Show |
intron_variant | MODIFIER | c.1921+779delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140658808 | |||||||
chr4:140659166 | A | C | 1 | a0001c0001t0003g0289 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1921+422T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659166 | |||||||
chr4:140659318 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1921+270G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659318 | |||||||
chr4:140659407 | C | T | 44 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0016 others(41): Show |
44 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(41): Show |
intron_variant | MODIFIER | c.1921+181G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659407 | |||||||
chr4:140659549 | C | T | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1921+39G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 11/20 | chr4 | 140659549 | |||||||
chr4:140659776 | T | G | 1 | a0001c0003t0001g0038 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1804-71A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140659776 | |||||||
chr4:140659880 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1804-175G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140659880 | |||||||
chr4:140660052 | C | T | 14 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(11): Show |
14 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1804-347G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660052 | |||||||
chr4:140660227 | G | A | 1 | a0001c0002t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1804-522C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660227 | |||||||
chr4:140660327 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1804-622G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660327 | |||||||
chr4:140660424 | G | A | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1804-719C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660424 | |||||||
chr4:140660451 | T | A | 1 | a0001c0010t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1804-746A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660451 | |||||||
chr4:140660573 | G | C | 2 | a0001c0001t0001g0004 a0001c0016t0012g0272 |
2 | HG02280.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.1804-868C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660573 | |||||||
chr4:140660607 | C | T | 1 | a0001c0003t0001g0194 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1804-902G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660607 | |||||||
chr4:140660617 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1804-912A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660617 | |||||||
chr4:140660671 | G | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0003g0287 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1804-966C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660671 | |||||||
chr4:140660676 | G | C | 182 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(179): Show |
182 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1804-971C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660676 | |||||||
chr4:140660685 | T | C | 2 | a0001c0004t0001g0143 a0001c0021t0001g0265 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1804-980A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660685 | |||||||
chr4:140660822 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1803+1071G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660822 | |||||||
chr4:140660833 | G | A | 1 | a0001c0001t0001g0199 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1803+1060C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660833 | |||||||
chr4:140660886 | G | C | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1803+1007C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660886 | |||||||
chr4:140660917 | C | CT | 104 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(101): Show |
104 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.1803+975dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660917 | |||||||
chr4:140660917 | C | CTT | 34 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0052 others(31): Show |
34 | HG00639.hp1 HG01257.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.1803+974_1803+975d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660917 | |||||||
chr4:140660954 | G | A | 4 | a0001c0005t0001g0130 a0001c0005t0001g0172 a0001c0005t0002g0128 others(1): Show |
4 | HG00639.hp1 HG02300.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1803+939C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660954 | |||||||
chr4:140660960 | G | T | 1 | a0001c0001t0001g0218 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1803+933C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660960 | |||||||
chr4:140660987 | T | C | 5 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1803+906A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140660987 | |||||||
chr4:140661035 | C | T | 1 | a0001c0004t0002g0127 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1803+858G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661035 | |||||||
chr4:140661039 | C | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1803+854G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661039 | |||||||
chr4:140661063 | T | C | 180 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(177): Show |
180 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.1803+830A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661063 | |||||||
chr4:140661072 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1803+821C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661072 | |||||||
chr4:140661107 | T | C | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1803+786A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661107 | |||||||
chr4:140661108 | G | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1803+785C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661108 | |||||||
chr4:140661131 | G | T | 7 | a0001c0001t0001g0162 a0001c0001t0001g0267 a0001c0001t0001g0271 others(4): Show |
7 | HG02258.hp2 HG02451.hp1 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803+762C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661131 | |||||||
chr4:140661150 | G | A | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1803+743C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661150 | |||||||
chr4:140661165 | T | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(206): Show |
209 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.1803+728A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661165 | |||||||
chr4:140661214 | G | A | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1803+679C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661214 | |||||||
chr4:140661236 | T | A | 8 | a0001c0005t0001g0146 a0001c0005t0001g0158 a0001c0008t0001g0180 others(5): Show |
8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.1803+657A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661236 | |||||||
chr4:140661286 | G | C | 35 | a0001c0001t0001g0064 a0001c0001t0002g0244 a0001c0003t0001g0009 others(32): Show |
35 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1803+607C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661286 | |||||||
chr4:140661346 | T | C | 6 | a0001c0004t0001g0143 a0001c0004t0005g0266 a0001c0013t0011g0116 others(3): Show |
6 | HG02559.hp1 HG02886.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+547A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661346 | |||||||
chr4:140661431 | C | T | 6 | a0001c0001t0001g0012 a0001c0002t0001g0224 a0001c0003t0001g0254 others(3): Show |
6 | HG00423.hp1 NA18948.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.1803+462G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661431 | |||||||
chr4:140661593 | C | T | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1803+300G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661593 | |||||||
chr4:140661690 | G | T | 19 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(16): Show |
19 | HG00639.hp1 HG01361.hp2 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.1803+203C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661690 | |||||||
chr4:140661755 | G | A | 1 | a0001c0001t0004g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1803+138C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 10/20 | chr4 | 140661755 | |||||||
chr4:140662385 | C | T | 2 | a0001c0004t0001g0153 a0001c0012t0008g0147 |
2 | HG03225.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1589-278G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662385 | |||||||
chr4:140662673 | T | C | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1589-566A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662673 | |||||||
chr4:140662738 | T | A | 37 | a0001c0001t0001g0064 a0001c0003t0001g0009 a0001c0004t0001g0047 others(34): Show |
37 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1589-631A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662738 | |||||||
chr4:140662800 | T | A | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1589-693A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662800 | |||||||
chr4:140662801 | A | G | 24 | a0001c0005t0001g0115 a0001c0005t0001g0129 a0001c0005t0001g0130 others(21): Show |
24 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.1589-694T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662801 | |||||||
chr4:140662811 | C | G | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1589-704G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140662811 | |||||||
chr4:140663028 | C | T | 23 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-921G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663028 | |||||||
chr4:140663484 | G | A | 26 | a0001c0001t0001g0012 a0001c0001t0001g0050 a0001c0002t0001g0095 others(23): Show |
26 | HG00423.hp1 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.1589-1377C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663484 | |||||||
chr4:140663510 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(178): Show |
181 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(178): Show |
intron_variant | MODIFIER | c.1589-1403G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663510 | |||||||
chr4:140663514 | T | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0140 a0001c0001t0001g0141 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1589-1407A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663514 | |||||||
chr4:140663603 | G | A | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1589-1496C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663603 | |||||||
chr4:140663882 | T | C | 2 | a0001c0004t0001g0143 a0001c0021t0001g0265 |
2 | HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1589-1775A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663882 | |||||||
chr4:140663912 | T | C | 36 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0140 others(33): Show |
36 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.1589-1805A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663912 | |||||||
chr4:140663977 | T | C | 23 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-1870A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140663977 | |||||||
chr4:140664039 | C | CA | 5 | a0001c0001t0001g0016 a0001c0001t0001g0077 a0001c0001t0001g0166 others(2): Show |
5 | HG02738.hp2 NA18981.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.1589-1933_1589-193 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664039 | |||||||
chr4:140664040 | C | A | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.1589-1933G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664040 | |||||||
chr4:140664040 | C | CA | 24 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0164 others(21): Show |
24 | HG00733.hp1 HG01070.hp2 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.1589-1934dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664040 | |||||||
chr4:140664209 | C | T | 1 | a0001c0002t0015g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1589-2102G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664209 | |||||||
chr4:140664215 | C | A | 1 | a0001c0006t0001g0213 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1589-2108G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664215 | |||||||
chr4:140664283 | AC | A | 23 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1589-2177delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664283 | |||||||
chr4:140664705 | CA | C | 7 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(4): Show |
7 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.1589-2599delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664705 | |||||||
chr4:140664768 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0140 a0001c0001t0001g0141 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1589-2661G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664768 | |||||||
chr4:140664831 | G | A | 1 | a0001c0001t0001g0249 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1589-2724C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664831 | |||||||
chr4:140664973 | G | T | 23 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(20): Show |
23 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1589-2866C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664973 | |||||||
chr4:140664989 | C | A | 2 | a0001c0001t0001g0271 a0001c0001t0002g0270 |
2 | HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1589-2882G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140664989 | |||||||
chr4:140665022 | G | T | 23 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(20): Show |
23 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1589-2915C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665022 | |||||||
chr4:140665051 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1589-2944C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665051 | |||||||
chr4:140665071 | C | T | 47 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(44): Show |
47 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.1589-2964G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665071 | |||||||
chr4:140665109 | G | GA | 8 | a0001c0001t0004g0292 a0001c0001t0010g0055 a0001c0003t0001g0084 others(5): Show |
8 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1589-3003dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665109 | |||||||
chr4:140665277 | C | T | 1 | a0001c0006t0001g0019 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1589-3170G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665277 | |||||||
chr4:140665368 | G | A | 1 | a0001c0002t0002g0221 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1589-3261C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665368 | |||||||
chr4:140665495 | T | C | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1589-3388A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665495 | |||||||
chr4:140665693 | C | T | 145 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(142): Show |
145 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1588+3224G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665693 | |||||||
chr4:140665752 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1588+3165A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665752 | |||||||
chr4:140665823 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1588+3094G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140665823 | |||||||
chr4:140666086 | G | A | 37 | a0001c0001t0001g0064 a0001c0003t0001g0009 a0001c0004t0001g0047 others(34): Show |
37 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.1588+2831C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666086 | |||||||
chr4:140666088 | A | G | 98 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1588+2829T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666088 | |||||||
chr4:140666095 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1588+2822C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666095 | |||||||
chr4:140666110 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1588+2807A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666110 | |||||||
chr4:140666139 | G | C | 47 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(44): Show |
47 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(44): Show |
intron_variant | MODIFIER | c.1588+2778C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666139 | |||||||
chr4:140666374 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0140 a0001c0001t0001g0141 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.1588+2543G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666374 | |||||||
chr4:140666460 | C | T | 1 | a0001c0004t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1588+2457G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666460 | |||||||
chr4:140666480 | C | A | 2 | a0001c0001t0001g0003 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1588+2437G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666480 | |||||||
chr4:140666523 | A | T | 1 | a0002c0009t0002g0121 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1588+2394T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666523 | |||||||
chr4:140666627 | C | A | 23 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(20): Show |
23 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(20): Show |
intron_variant | MODIFIER | c.1588+2290G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666627 | |||||||
chr4:140666629 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1588+2288G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666629 | |||||||
chr4:140666734 | T | TA | 36 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0002g0274 others(33): Show |
36 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.1588+2182dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666734 | |||||||
chr4:140666734 | T | TAA | 37 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(34): Show |
37 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1588+2181_1588+218 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666734 | |||||||
chr4:140666734 | T | TAAAA | 94 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.1588+2179_1588+218 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666734 | |||||||
chr4:140666743 | A | G | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1588+2174T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666743 | |||||||
chr4:140666821 | G | GAT | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1588+2094_1588+209 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666821 | |||||||
chr4:140666884 | C | A | 23 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
23 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1588+2033G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140666884 | |||||||
chr4:140667160 | G | A | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.1588+1757C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667160 | |||||||
chr4:140667287 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0001g0251 |
2 | HG02738.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.1588+1630C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667287 | |||||||
chr4:140667315 | T | A | 2 | a0001c0004t0005g0266 a0001c0013t0011g0116 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1588+1602A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667315 | |||||||
chr4:140667324 | G | A | 1 | a0001c0004t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1588+1593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667324 | |||||||
chr4:140667349 | C | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1588+1568G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667349 | |||||||
chr4:140667461 | C | G | 1 | a0001c0005t0001g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1588+1456G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667461 | |||||||
chr4:140667557 | G | A | 3 | a0001c0004t0005g0266 a0001c0013t0011g0116 a0001c0020t0001g0188 |
3 | HG02886.hp1 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1588+1360C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667557 | |||||||
chr4:140667653 | C | G | 20 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(17): Show |
20 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+1264G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667653 | |||||||
chr4:140667939 | C | T | 25 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(22): Show |
25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.1588+978G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667939 | |||||||
chr4:140667959 | T | C | 26 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(23): Show |
26 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.1588+958A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667959 | |||||||
chr4:140667990 | A | G | 1 | a0001c0014t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1588+927T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140667990 | |||||||
chr4:140668110 | G | T | 20 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(17): Show |
20 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+807C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668110 | |||||||
chr4:140668147 | G | A | 187 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(184): Show |
187 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1588+770C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668147 | |||||||
chr4:140668168 | G | A | 20 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(17): Show |
20 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(17): Show |
intron_variant | MODIFIER | c.1588+749C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668168 | |||||||
chr4:140668225 | T | C | 22 | a0001c0004t0001g0143 a0001c0005t0001g0115 a0001c0005t0001g0129 others(19): Show |
22 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.1588+692A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668225 | |||||||
chr4:140668509 | A | G | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1588+408T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668509 | |||||||
chr4:140668527 | T | C | 1 | a0001c0005t0001g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1588+390A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668527 | |||||||
chr4:140668532 | T | G | 3 | a0001c0004t0005g0266 a0001c0013t0011g0116 a0001c0020t0001g0188 |
3 | HG02886.hp1 HG02896.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1588+385A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668532 | |||||||
chr4:140668552 | A | T | 1 | a0001c0002t0001g0095 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1588+365T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668552 | |||||||
chr4:140668888 | C | T | 2 | a0001c0001t0001g0059 a0001c0007t0001g0230 |
2 | HG03710.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.1588+29G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668888 | |||||||
chr4:140668889 | G | A | 11 | a0001c0002t0001g0051 a0001c0002t0001g0189 a0001c0002t0001g0197 others(8): Show |
11 | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588+28C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 9/20 | chr4 | 140668889 | |||||||
chr4:140669087 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1438-20T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 8/20 | chr4 | 140669087 | |||||||
chr4:140669160 | C | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1438-93G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 8/20 | chr4 | 140669160 | |||||||
chr4:140669332 | C | G | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1438-265G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 8/20 | chr4 | 140669332 | |||||||
chr4:140669937 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1267-133G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140669937 | |||||||
chr4:140670322 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1266+398T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670322 | |||||||
chr4:140670557 | C | T | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1266+163G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670557 | |||||||
chr4:140670615 | G | A | 12 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(9): Show |
12 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.1266+105C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670615 | |||||||
chr4:140670704 | G | T | 1 | a0001c0004t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1266+16C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 7/20 | chr4 | 140670704 | |||||||
chr4:140670972 | C | G | 2 | a0001c0001t0014g0284 a0001c0003t0003g0285 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-46G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140670972 | |||||||
chr4:140671052 | A | G | 167 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(164): Show |
167 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(164): Show |
intron_variant | MODIFIER | c.1060-126T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671052 | |||||||
chr4:140671071 | G | C | 2 | a0001c0003t0001g0084 a0001c0015t0002g0085 |
2 | NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1060-145C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671071 | |||||||
chr4:140671139 | G | A | 2 | a0001c0004t0005g0266 a0001c0013t0011g0116 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1060-213C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671139 | |||||||
chr4:140671219 | T | G | 151 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(148): Show |
151 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(148): Show |
intron_variant | MODIFIER | c.1060-293A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671219 | |||||||
chr4:140671416 | A | G | 97 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(94): Show |
97 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.1060-490T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671416 | |||||||
chr4:140671550 | T | C | 2 | a0001c0005t0001g0160 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1060-624A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671550 | |||||||
chr4:140671669 | C | T | 1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060-743G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671669 | |||||||
chr4:140671674 | C | CTG | 41 | a0001c0001t0001g0007 a0001c0001t0001g0012 a0001c0001t0001g0033 others(38): Show |
41 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(38): Show |
intron_variant | MODIFIER | c.1060-750_1060-749d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTG | 16 | a0001c0001t0001g0024 a0001c0001t0001g0035 a0001c0001t0001g0050 others(13): Show |
16 | HG01175.hp2 HG01255.hp2 HG01257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1060-752_1060-749d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTG | 5 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0002g0274 others(2): Show |
5 | HG02965.hp2 HG03453.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-754_1060-749d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(1): Show |
7 | a0001c0001t0001g0036 a0001c0001t0001g0238 a0001c0001t0002g0157 others(4): Show |
7 | HG00642.hp1 HG02055.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1060-756_1060-749d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(3): Show |
1 | a0001c0008t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1060-758_1060-749d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(5): Show |
11 | a0001c0001t0001g0139 a0001c0002t0001g0268 a0001c0002t0001g0269 others(8): Show |
11 | HG02451.hp2 HG02630.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1060-760_1060-749d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(7): Show |
4 | a0001c0001t0001g0091 a0001c0001t0001g0149 a0001c0001t0001g0154 others(1): Show |
4 | HG01884.hp2 HG01891.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-762_1060-749d others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(9): Show |
7 | a0001c0001t0001g0094 a0001c0001t0001g0148 a0001c0001t0001g0150 others(4): Show |
7 | HG01192.hp1 HG02717.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-764_1060-749d others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(11): Show |
6 | a0001c0001t0001g0004 a0001c0001t0001g0093 a0001c0001t0001g0145 others(3): Show |
6 | HG02280.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-766_1060-749d others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | C | CTGTGTGT others(13): Show |
1 | a0001c0001t0001g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1060-768_1060-749d others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | CTG | C | 97 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(94): Show |
97 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1060-750_1060-749d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | CTGTG | C | 4 | a0001c0004t0001g0143 a0001c0004t0001g0169 a0001c0005t0001g0115 others(1): Show |
5 | HG01256.hp1 HG01258.hp2 HG02056.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-752_1060-749d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | CTGTGTG | C | 4 | a0001c0004t0005g0266 a0001c0007t0007g0107 a0001c0013t0011g0116 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-754_1060-749d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | CTGTGTGT others(1): Show |
C | 44 | a0001c0004t0001g0047 a0001c0004t0001g0105 a0001c0004t0001g0108 others(41): Show |
44 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.1060-756_1060-749d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671674 | CTGTGTGT others(3): Show |
C | 4 | a0001c0001t0001g0003 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG03209.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1060-758_1060-749d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671674 | |||||||
chr4:140671712 | G | GTGTA | 3 | a0001c0001t0001g0177 a0001c0001t0001g0267 a0001c0001t0006g0142 |
3 | HG02055.hp2 HG02451.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671712 | G | GTGTGTGT others(1): Show |
4 | a0001c0001t0001g0161 a0001c0001t0001g0178 a0001c0002t0001g0245 others(1): Show |
4 | HG01106.hp2 HG02258.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-787_1060-786i others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671712 | G | GTGTGTGT others(3): Show |
1 | a0001c0003t0003g0285 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1060-787_1060-786i others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671712 | G | GTGTGTGT others(5): Show |
3 | a0001c0001t0014g0284 a0001c0004t0001g0229 a0001c0004t0002g0261 |
3 | HG02723.hp1 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671712 | G | GTGTGTGT others(7): Show |
3 | a0001c0001t0001g0271 a0001c0001t0002g0270 a0001c0001t0017g0297 |
3 | HG02258.hp2 HG02647.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671712 | G | GTGTGTGT others(9): Show |
3 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0016t0012g0272 |
3 | HG01070.hp2 HG01071.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.1060-787_1060-786i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671712 | G | GTGTGTGT others(13): Show |
1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1060-787_1060-786i others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671712 | |||||||
chr4:140671902 | T | C | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1060-976A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671902 | |||||||
chr4:140671987 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-1061A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140671987 | |||||||
chr4:140672078 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1060-1152A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672078 | |||||||
chr4:140672159 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1060-1233C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672159 | |||||||
chr4:140672198 | A | G | 15 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(12): Show |
15 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(12): Show |
intron_variant | MODIFIER | c.1060-1272T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672198 | |||||||
chr4:140672349 | T | C | 186 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(183): Show |
186 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(183): Show |
intron_variant | MODIFIER | c.1060-1423A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672349 | |||||||
chr4:140672468 | T | G | 2 | a0001c0005t0001g0160 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1060-1542A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672468 | |||||||
chr4:140672483 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1060-1557C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672483 | |||||||
chr4:140672561 | T | C | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.1060-1635A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672561 | |||||||
chr4:140672709 | A | G | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1060-1783T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672709 | |||||||
chr4:140672721 | C | A | 19 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG00544.hp1 HG00558.hp1 HG01167.hp2 others(16): Show |
intron_variant | MODIFIER | c.1060-1795G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672721 | |||||||
chr4:140672862 | T | A | 1 | a0001c0001t0002g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1060-1936A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672862 | |||||||
chr4:140672869 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1060-1943A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672869 | |||||||
chr4:140672890 | T | C | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1060-1964A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672890 | |||||||
chr4:140672926 | T | A | 20 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0161 others(17): Show |
20 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1060-2000A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140672926 | |||||||
chr4:140673167 | C | CA | 7 | a0001c0001t0001g0162 a0001c0001t0001g0271 a0001c0001t0002g0270 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.1060-2242dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673167 | |||||||
chr4:140673167 | CA | C | 124 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.1060-2242delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673167 | |||||||
chr4:140673185 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-2259A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673185 | |||||||
chr4:140673265 | G | C | 1 | a0001c0008t0001g0180 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1060-2339C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673265 | |||||||
chr4:140673304 | C | A | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1060-2378G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673304 | |||||||
chr4:140673486 | A | C | 1 | a0001c0002t0001g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1060-2560T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673486 | |||||||
chr4:140673499 | G | A | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
271 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.1060-2573C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673499 | |||||||
chr4:140673598 | A | G | 3 | a0001c0004t0001g0087 a0001c0004t0005g0266 a0001c0013t0011g0116 |
3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1060-2672T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673598 | |||||||
chr4:140673751 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1060-2825T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673751 | |||||||
chr4:140673949 | T | C | 39 | a0001c0004t0001g0047 a0001c0004t0001g0087 a0001c0004t0001g0105 others(36): Show |
39 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1059+2945A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140673949 | |||||||
chr4:140674170 | G | C | 3 | a0001c0002t0001g0207 a0001c0002t0001g0215 a0001c0002t0001g0235 |
3 | HG00609.hp2 HG00673.hp1 NA19063.hp2 |
intron_variant | MODIFIER | c.1059+2724C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674170 | |||||||
chr4:140674279 | T | C | 1 | a0001c0001t0001g0152 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1059+2615A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674279 | |||||||
chr4:140674333 | T | C | 1 | a0001c0001t0001g0070 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1059+2561A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674333 | |||||||
chr4:140674353 | C | G | 2 | a0001c0001t0001g0091 a0001c0001t0001g0154 |
2 | HG01891.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1059+2541G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674353 | |||||||
chr4:140674529 | T | G | 3 | a0001c0001t0001g0082 a0001c0003t0001g0084 a0001c0015t0002g0085 |
3 | NA18941.hp1 NA18987.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1059+2365A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674529 | |||||||
chr4:140674597 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+2297A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674597 | |||||||
chr4:140674676 | A | AAT | 39 | a0001c0001t0001g0003 a0001c0004t0001g0047 a0001c0004t0001g0087 others(36): Show |
39 | HG00408.hp2 HG00558.hp2 HG00741.hp1 others(36): Show |
intron_variant | MODIFIER | c.1059+2216_1059+221 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674676 | |||||||
chr4:140674676 | A | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+2218T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674676 | |||||||
chr4:140674687 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1059+2207T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674687 | |||||||
chr4:140674691 | A | AT | 9 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(6): Show |
9 | HG01361.hp2 HG02300.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.1059+2202dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674691 | |||||||
chr4:140674691 | A | T | 15 | a0001c0001t0001g0012 a0001c0002t0001g0098 a0001c0002t0001g0100 others(12): Show |
15 | HG00099.hp1 HG00423.hp1 HG00673.hp1 others(12): Show |
intron_variant | MODIFIER | c.1059+2203T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674691 | |||||||
chr4:140674692 | T | TA | 18 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(15): Show |
18 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(15): Show |
intron_variant | MODIFIER | c.1059+2201_1059+220 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674692 | |||||||
chr4:140674693 | T | A | 42 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0050 others(39): Show |
42 | HG00639.hp2 HG01074.hp2 HG01106.hp1 others(39): Show |
intron_variant | MODIFIER | c.1059+2201A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674693 | |||||||
chr4:140674694 | T | A | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1059+2200A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674694 | |||||||
chr4:140674704 | T | C | 70 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(67): Show |
70 | HG00408.hp2 HG00558.hp2 HG00639.hp1 others(67): Show |
intron_variant | MODIFIER | c.1059+2190A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674704 | |||||||
chr4:140674791 | T | C | 1 | a0001c0002t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1059+2103A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674791 | |||||||
chr4:140674836 | C | T | 31 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(28): Show |
31 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.1059+2058G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674836 | |||||||
chr4:140674862 | C | T | 3 | a0001c0004t0001g0087 a0001c0004t0005g0266 a0001c0013t0011g0116 |
3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1059+2032G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674862 | |||||||
chr4:140674868 | T | G | 150 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1059+2026A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674868 | |||||||
chr4:140674960 | C | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+1934G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674960 | |||||||
chr4:140674994 | C | T | 150 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(147): Show |
150 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.1059+1900G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140674994 | |||||||
chr4:140675008 | C | A | 2 | a0001c0005t0001g0160 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1059+1886G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675008 | |||||||
chr4:140675210 | G | A | 2 | a0001c0008t0001g0241 a0001c0008t0005g0242 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1059+1684C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675210 | |||||||
chr4:140675234 | A | AC | 223 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(220): Show |
223 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(220): Show |
intron_variant | MODIFIER | c.1059+1659_1059+166 others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675234 | |||||||
chr4:140675498 | C | A | 5 | a0001c0002t0001g0101 a0001c0002t0001g0106 a0001c0002t0006g0099 others(2): Show |
5 | HG00735.hp1 HG01884.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1059+1396G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675498 | |||||||
chr4:140675537 | G | C | 1 | a0001c0002t0001g0211 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1059+1357C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675537 | |||||||
chr4:140675563 | T | A | 7 | a0001c0001t0001g0010 a0001c0001t0001g0073 a0001c0001t0001g0192 others(4): Show |
7 | HG00408.hp1 HG00544.hp2 HG00673.hp2 others(4): Show |
intron_variant | MODIFIER | c.1059+1331A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675563 | |||||||
chr4:140675616 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1059+1278A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675616 | |||||||
chr4:140675631 | T | G | 25 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(22): Show |
25 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(22): Show |
intron_variant | MODIFIER | c.1059+1263A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675631 | |||||||
chr4:140675836 | C | A | 33 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(30): Show |
33 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(30): Show |
intron_variant | MODIFIER | c.1059+1058G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140675836 | |||||||
chr4:140676241 | G | A | 1 | a0001c0001t0001g0052 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.1059+653C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676241 | |||||||
chr4:140676259 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1059+635G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676259 | |||||||
chr4:140676267 | G | A | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1059+627C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676267 | |||||||
chr4:140676626 | G | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1059+268C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676626 | |||||||
chr4:140676733 | T | C | 4 | a0001c0001t0001g0139 a0001c0001t0001g0238 a0001c0001t0002g0157 others(1): Show |
4 | HG02055.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+161A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676733 | |||||||
chr4:140676759 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.1059+135T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 6/20 | chr4 | 140676759 | |||||||
chr4:140677136 | A | G | 41 | a0001c0004t0001g0047 a0001c0004t0001g0087 a0001c0004t0001g0105 others(38): Show |
41 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.852-35T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677136 | |||||||
chr4:140677168 | G | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0162 others(23): Show |
26 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.852-67C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677168 | |||||||
chr4:140677407 | A | G | 41 | a0001c0004t0001g0047 a0001c0004t0001g0087 a0001c0004t0001g0105 others(38): Show |
41 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.852-306T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677407 | |||||||
chr4:140677645 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.852-544A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677645 | |||||||
chr4:140677693 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.852-592G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677693 | |||||||
chr4:140677707 | C | T | 2 | a0001c0002t0001g0210 a0001c0002t0001g0223 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.852-606G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677707 | |||||||
chr4:140677771 | C | T | 2 | a0001c0002t0001g0245 a0001c0021t0001g0265 |
2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.852-670G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677771 | |||||||
chr4:140677874 | T | C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.852-773A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677874 | |||||||
chr4:140677882 | C | T | 2 | a0001c0005t0001g0160 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.852-781G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140677882 | |||||||
chr4:140678018 | T | TA | 144 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(141): Show |
144 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(141): Show |
intron_variant | MODIFIER | c.852-918dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678018 | |||||||
chr4:140678206 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.851+736A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678206 | |||||||
chr4:140678285 | T | C | 34 | a0001c0004t0001g0047 a0001c0004t0001g0105 a0001c0004t0001g0108 others(31): Show |
34 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.851+657A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678285 | |||||||
chr4:140678324 | C | T | 15 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(12): Show |
15 | HG01192.hp1 HG01891.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.851+618G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678324 | |||||||
chr4:140678533 | G | T | 1 | a0001c0008t0005g0179 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.851+409C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678533 | |||||||
chr4:140678544 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(117): Show |
120 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.851+398G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678544 | |||||||
chr4:140678687 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.851+255A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678687 | |||||||
chr4:140678859 | G | A | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.851+83C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 5/20 | chr4 | 140678859 | |||||||
chr4:140679218 | C | T | 2 | a0001c0001t0003g0287 a0001c0001t0003g0288 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.590-15G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/20 | chr4 | 140679218 | |||||||
chr4:140679390 | T | C | 31 | a0001c0004t0001g0047 a0001c0004t0001g0105 a0001c0004t0001g0108 others(28): Show |
31 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.590-187A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/20 | chr4 | 140679390 | |||||||
chr4:140679486 | T | TA | 26 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(23): Show |
26 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(23): Show |
intron_variant | MODIFIER | c.589+128dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 4/20 | chr4 | 140679486 | |||||||
chr4:140679935 | T | TA | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.361-93dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140679935 | |||||||
chr4:140680035 | A | G | 1 | a0001c0004t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.361-192T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680035 | |||||||
chr4:140680266 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.361-423G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680266 | |||||||
chr4:140680440 | G | A | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-597C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680440 | |||||||
chr4:140680530 | G | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-687C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680530 | |||||||
chr4:140680538 | A | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.361-695T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680538 | |||||||
chr4:140680603 | C | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0192 |
2 | HG00544.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.361-760G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680603 | |||||||
chr4:140680768 | T | C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.361-925A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680768 | |||||||
chr4:140680859 | G | A | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.361-1016C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680859 | |||||||
chr4:140680900 | T | C | 1 | a0001c0002t0001g0112 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.361-1057A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140680900 | |||||||
chr4:140681342 | A | G | 1 | a0001c0002t0002g0092 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.361-1499T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681342 | |||||||
chr4:140681520 | A | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.361-1677T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681520 | |||||||
chr4:140681529 | A | T | 46 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(43): Show |
46 | HG00639.hp1 HG01070.hp2 HG01071.hp2 others(43): Show |
intron_variant | MODIFIER | c.361-1686T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681529 | |||||||
chr4:140681575 | C | A | 1 | a0001c0001t0001g0257 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.361-1732G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681575 | |||||||
chr4:140681904 | A | G | 25 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(22): Show |
25 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.361-2061T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681904 | |||||||
chr4:140681920 | C | G | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.361-2077G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140681920 | |||||||
chr4:140682165 | A | G | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-2322T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682165 | |||||||
chr4:140682203 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.361-2360A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682203 | |||||||
chr4:140682315 | T | C | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
271 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(268): Show |
intron_variant | MODIFIER | c.361-2472A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682315 | |||||||
chr4:140682342 | G | A | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.361-2499C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682342 | |||||||
chr4:140682515 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.361-2672C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682515 | |||||||
chr4:140682823 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.361-2980T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682823 | |||||||
chr4:140682949 | C | T | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.361-3106G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140682949 | |||||||
chr4:140683044 | G | A | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.361-3201C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683044 | |||||||
chr4:140683167 | C | T | 1 | a0001c0004t0005g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.360+3177G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683167 | |||||||
chr4:140683404 | T | C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.360+2940A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683404 | |||||||
chr4:140683418 | C | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.360+2926G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683418 | |||||||
chr4:140683431 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+2913A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683431 | |||||||
chr4:140683492 | G | A | 146 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(143): Show |
146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.360+2852C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683492 | |||||||
chr4:140683725 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(210): Show |
213 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.360+2619A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683725 | |||||||
chr4:140683798 | T | G | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.360+2546A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683798 | |||||||
chr4:140683802 | G | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0271 a0001c0001t0002g0270 others(3): Show |
6 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.360+2542C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140683802 | |||||||
chr4:140684240 | TA | T | 64 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(61): Show |
64 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(61): Show |
intron_variant | MODIFIER | c.360+2103delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684240 | |||||||
chr4:140684323 | A | G | 25 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(22): Show |
25 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.360+2021T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684323 | |||||||
chr4:140684554 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.360+1790A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684554 | |||||||
chr4:140684570 | T | C | 2 | a0001c0005t0002g0103 a0001c0005t0002g0104 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.360+1774A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684570 | |||||||
chr4:140684712 | A | G | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.360+1632T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684712 | |||||||
chr4:140684733 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.360+1611C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684733 | |||||||
chr4:140684872 | AG | A | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.360+1471delC | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140684872 | |||||||
chr4:140685130 | C | G | 1 | a0003c0019t0002g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.360+1214G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685130 | |||||||
chr4:140685149 | A | G | 1 | a0001c0004t0001g0153 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.360+1195T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685149 | |||||||
chr4:140685175 | C | G | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.360+1169G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685175 | |||||||
chr4:140685218 | T | C | 2 | a0001c0008t0001g0241 a0001c0008t0005g0242 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.360+1126A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685218 | |||||||
chr4:140685431 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.360+913G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685431 | |||||||
chr4:140685432 | G | A | 36 | a0001c0004t0001g0047 a0001c0004t0001g0105 a0001c0004t0001g0108 others(33): Show |
36 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.360+912C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685432 | |||||||
chr4:140685530 | C | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.360+814G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685530 | |||||||
chr4:140685805 | T | A | 4 | a0001c0002t0001g0098 a0001c0002t0001g0100 a0001c0002t0001g0181 others(1): Show |
4 | HG02145.hp2 HG02622.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.360+539A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685805 | |||||||
chr4:140685914 | C | T | 119 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(116): Show |
119 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.360+430G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685914 | |||||||
chr4:140685938 | TAAC | T | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.360+403_360+405del others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140685938 | |||||||
chr4:140686098 | A | G | 1 | a0001c0002t0001g0202 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.360+246T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140686098 | |||||||
chr4:140686256 | G | C | 5 | a0001c0004t0001g0087 a0001c0004t0001g0229 a0001c0004t0002g0261 others(2): Show |
5 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.360+88C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 3/20 | chr4 | 140686256 | |||||||
chr4:140686525 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.242-63G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686525 | |||||||
chr4:140686603 | C | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-141G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686603 | |||||||
chr4:140686628 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-166A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686628 | |||||||
chr4:140686644 | C | T | 2 | a0001c0003t0001g0072 a0001c0003t0001g0074 |
2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.242-182G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686644 | |||||||
chr4:140686645 | G | A | 2 | a0001c0008t0001g0241 a0001c0008t0005g0242 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.242-183C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686645 | |||||||
chr4:140686822 | G | C | 1 | a0001c0008t0005g0242 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.242-360C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140686822 | |||||||
chr4:140687153 | A | C | 1 | a0001c0001t0001g0035 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.242-691T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687153 | |||||||
chr4:140687242 | A | G | 5 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(2): Show |
5 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-780T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687242 | |||||||
chr4:140687321 | A | ATATG | 5 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0168 others(2): Show |
5 | HG00423.hp2 HG00544.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-860_242-859ins others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | |||||||
chr4:140687321 | A | ATATGTG | 73 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(70): Show |
73 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.242-860_242-859ins others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | |||||||
chr4:140687321 | A | ATGTGTG | 3 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0003g0278 |
3 | HG01975.hp1 HG01978.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.242-865_242-860dup others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | |||||||
chr4:140687321 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.242-859T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687321 | |||||||
chr4:140687323 | G | A | 19 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0034 others(16): Show |
19 | HG00621.hp1 HG00642.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.242-861C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687323 | |||||||
chr4:140687338 | TGTGTCAT others(31): Show |
T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-914_242-877del others(38): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687338 | |||||||
chr4:140687341 | GTCA | G | 25 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0091 others(22): Show |
25 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.242-882_242-880del others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | |||||||
chr4:140687341 | GTCATA | G | 9 | a0001c0001t0001g0166 a0001c0001t0001g0176 a0001c0001t0002g0067 others(6): Show |
9 | HG02738.hp2 HG04199.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-884_242-880del others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | |||||||
chr4:140687341 | GTCATATA | G | 37 | a0001c0001t0001g0141 a0001c0001t0001g0164 a0001c0001t0002g0090 others(34): Show |
37 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(34): Show |
intron_variant | MODIFIER | c.242-886_242-880del others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | |||||||
chr4:140687341 | GTCATATA others(18): Show |
G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0063 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.242-904_242-880del others(25): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687341 | |||||||
chr4:140687342 | T | TGTCATAT others(3): Show |
1 | a0001c0001t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.242-881_242-880ins others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(5): Show |
1 | a0001c0001t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(7): Show |
3 | a0001c0001t0001g0212 a0001c0001t0003g0279 a0001c0001t0004g0296 |
3 | HG03834.hp2 NA18963.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.242-881_242-880ins others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(9): Show |
1 | a0001c0001t0016g0295 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(11): Show |
1 | a0001c0001t0004g0294 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.242-881_242-880ins others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(15): Show |
1 | a0001c0001t0004g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.242-881_242-880ins others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(17): Show |
1 | a0001c0001t0001g0052 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(19): Show |
1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(26): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(25): Show |
2 | a0001c0001t0003g0289 a0001c0001t0004g0291 |
2 | NA19012.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.242-881_242-880ins others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTC others(27): Show |
1 | a0001c0003t0001g0072 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(34): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | T | TGTGTGTG others(7): Show |
1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.242-881_242-880ins others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | TC | T | 9 | a0001c0001t0001g0203 a0001c0001t0001g0208 a0001c0001t0002g0157 others(6): Show |
9 | HG00621.hp1 HG00642.hp2 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.242-881delG | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687342 | TCATATAT others(3): Show |
T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-890_242-881del others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687342 | |||||||
chr4:140687343 | C | CAT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0028 others(16): Show |
20 | HG00099.hp2 HG00423.hp1 HG01081.hp2 others(17): Show |
intron_variant | MODIFIER | c.242-883_242-882dup others(2): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | CATAT | 21 | a0001c0001t0001g0015 a0001c0001t0001g0045 a0001c0001t0001g0057 others(18): Show |
21 | HG00558.hp1 HG00609.hp1 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.242-885_242-882dup others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | CATATAT | 18 | a0001c0001t0001g0006 a0001c0001t0001g0010 a0001c0001t0001g0029 others(15): Show |
18 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(15): Show |
intron_variant | MODIFIER | c.242-887_242-882dup others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | CATATATA others(1): Show |
5 | a0001c0001t0001g0021 a0001c0001t0001g0077 a0001c0001t0001g0109 others(2): Show |
5 | HG00673.hp2 HG01243.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-889_242-882dup others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | CATATATA others(3): Show |
9 | a0001c0001t0001g0117 a0001c0001t0001g0123 a0001c0001t0001g0218 others(6): Show |
9 | HG00140.hp2 HG01496.hp2 HG02155.hp1 others(6): Show |
intron_variant | MODIFIER | c.242-891_242-882dup others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | CATATATA others(7): Show |
4 | a0001c0001t0001g0008 a0001c0001t0001g0016 a0001c0001t0001g0257 others(1): Show |
4 | HG01928.hp1 NA18972.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-895_242-882dup others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | CATATATA others(9): Show |
4 | a0001c0001t0001g0027 a0001c0001t0001g0032 a0001c0001t0001g0033 others(1): Show |
4 | HG01346.hp1 HG02004.hp2 HG02056.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-897_242-882dup others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | G | 5 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0113 others(2): Show |
5 | HG00423.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-881G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | C | T | 18 | a0001c0001t0001g0052 a0001c0001t0001g0195 a0001c0001t0001g0212 others(15): Show |
18 | HG01257.hp1 HG01261.hp2 HG02165.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-881G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CAT | C | 11 | a0001c0002t0001g0174 a0001c0002t0001g0196 a0001c0002t0001g0202 others(8): Show |
11 | HG01069.hp2 HG01123.hp1 HG01346.hp2 others(8): Show |
intron_variant | MODIFIER | c.242-883_242-882del others(2): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATAT | C | 7 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0002t0001g0243 others(4): Show |
7 | HG01243.hp1 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.242-885_242-882del others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATAT | C | 8 | a0001c0002t0001g0051 a0001c0002t0001g0181 a0001c0002t0001g0193 others(5): Show |
8 | HG00733.hp1 HG01070.hp1 HG01123.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-887_242-882del others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(1): Show |
C | 11 | a0001c0001t0014g0284 a0001c0002t0001g0098 a0001c0002t0001g0100 others(8): Show |
11 | HG00639.hp2 HG00673.hp1 HG01361.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-889_242-882del others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(3): Show |
C | 6 | a0001c0002t0001g0215 a0001c0002t0001g0224 a0001c0002t0001g0268 others(3): Show |
6 | HG00609.hp2 HG01081.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.242-891_242-882del others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(5): Show |
C | 4 | a0001c0002t0001g0101 a0001c0002t0006g0165 a0001c0003t0003g0285 others(1): Show |
4 | HG00735.hp1 HG02451.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.242-893_242-882del others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(7): Show |
C | 2 | a0001c0002t0001g0106 a0001c0002t0006g0099 |
2 | HG01884.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.242-895_242-882del others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(9): Show |
C | 4 | a0001c0001t0001g0177 a0001c0001t0001g0178 a0001c0001t0006g0142 others(1): Show |
4 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-897_242-882del others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(11): Show |
C | 3 | a0001c0001t0001g0161 a0001c0002t0003g0290 a0001c0016t0012g0272 |
3 | HG02559.hp1 HG02559.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.242-899_242-882del others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(13): Show |
C | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.242-901_242-882del others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(15): Show |
C | 8 | a0001c0001t0001g0162 a0001c0001t0001g0271 a0001c0001t0002g0270 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.242-903_242-882del others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687343 | CATATATA others(17): Show |
C | 8 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0134 others(5): Show |
8 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-905_242-882del others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687343 | |||||||
chr4:140687344 | A | G | 10 | a0001c0001t0001g0203 a0001c0001t0001g0208 a0001c0001t0002g0157 others(7): Show |
10 | HG00621.hp1 HG00642.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-882T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687344 | |||||||
chr4:140687344 | A | T | 5 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0113 others(2): Show |
5 | HG00423.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-882T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687344 | |||||||
chr4:140687345 | T | C | 5 | a0001c0001t0001g0035 a0001c0001t0001g0059 a0001c0001t0001g0113 others(2): Show |
5 | HG00423.hp2 HG00741.hp2 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-883A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687345 | |||||||
chr4:140687346 | A | G | 35 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0091 others(32): Show |
35 | HG00621.hp1 HG00642.hp2 HG01257.hp1 others(32): Show |
intron_variant | MODIFIER | c.242-884T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687346 | |||||||
chr4:140687348 | A | G | 43 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0091 others(40): Show |
43 | HG00621.hp1 HG00642.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.242-886T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687348 | |||||||
chr4:140687349 | T | G | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.242-887A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687349 | |||||||
chr4:140687349 | T | TC | 7 | a0001c0001t0001g0208 a0001c0003t0001g0042 a0001c0003t0001g0056 others(4): Show |
7 | HG00621.hp1 HG00642.hp2 HG04228.hp2 others(4): Show |
intron_variant | MODIFIER | c.242-888_242-887ins others(1): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687349 | |||||||
chr4:140687350 | A | G | 72 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0001t0001g0091 others(69): Show |
72 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.242-888T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687350 | |||||||
chr4:140687350 | A | T | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.242-888T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687350 | |||||||
chr4:140687351 | T | C | 2 | a0001c0001t0001g0203 a0001c0008t0001g0241 |
2 | NA18970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.242-889A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687351 | |||||||
chr4:140687351 | TA | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0018t0001g0175 |
3 | HG03710.hp2 NA19011.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.242-890delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687351 | |||||||
chr4:140687351 | TATATATA others(38): Show |
T | 1 | a0001c0003t0001g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.242-934_242-890del others(45): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687351 | |||||||
chr4:140687352 | A | G | 70 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(67): Show |
70 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.242-890T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687352 | |||||||
chr4:140687353 | T | C | 3 | a0001c0001t0001g0011 a0001c0001t0001g0034 a0001c0018t0001g0175 |
3 | HG03710.hp2 NA19011.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.242-891A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687353 | |||||||
chr4:140687353 | T | G | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-891A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687353 | |||||||
chr4:140687353 | TA | T | 68 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(65): Show |
68 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.242-892delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687353 | |||||||
chr4:140687354 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.242-892T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687354 | |||||||
chr4:140687354 | A | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-892T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687354 | |||||||
chr4:140687355 | T | C | 69 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(66): Show |
69 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.242-893A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687355 | |||||||
chr4:140687356 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.242-894T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687356 | |||||||
chr4:140687358 | A | G | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.242-896T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687358 | |||||||
chr4:140687360 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.242-898T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687360 | |||||||
chr4:140687361 | T | C | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.242-899A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687361 | |||||||
chr4:140687363 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.242-901A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687363 | |||||||
chr4:140687368 | A | G | 68 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0091 others(65): Show |
68 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.242-906T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687368 | |||||||
chr4:140687370 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0063 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.242-908T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687370 | |||||||
chr4:140687370 | A | T | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-908T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687370 | |||||||
chr4:140687372 | A | G | 2 | a0001c0001t0001g0007 a0001c0001t0001g0063 |
2 | HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.242-910T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687372 | |||||||
chr4:140687377 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-915A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687377 | |||||||
chr4:140687378 | A | G | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-916T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687378 | |||||||
chr4:140687380 | A | T | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-918T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687380 | |||||||
chr4:140687388 | A | G | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-926T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687388 | |||||||
chr4:140687389 | T | A | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-927A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687389 | |||||||
chr4:140687390 | A | C | 66 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(63): Show |
66 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(63): Show |
intron_variant | MODIFIER | c.242-928T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687390 | |||||||
chr4:140687396 | A | AT | 3 | a0001c0002t0001g0095 a0001c0002t0001g0197 a0001c0002t0001g0237 |
3 | HG01169.hp1 HG01169.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.242-935_242-934ins others(1): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687396 | |||||||
chr4:140687396 | A | G | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.242-934T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687396 | |||||||
chr4:140687397 | A | T | 2 | a0001c0001t0001g0006 a0001c0001t0001g0185 |
2 | HG01515.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.242-935T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687397 | |||||||
chr4:140687403 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-941A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687403 | |||||||
chr4:140687491 | T | A | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-1029A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687491 | |||||||
chr4:140687631 | C | T | 11 | a0001c0001t0001g0144 a0001c0001t0001g0145 a0001c0001t0001g0148 others(8): Show |
11 | HG01884.hp2 HG02572.hp1 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.242-1169G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140687631 | |||||||
chr4:140688138 | T | C | 15 | a0001c0001t0001g0161 a0001c0001t0001g0162 a0001c0001t0001g0177 others(12): Show |
15 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(12): Show |
intron_variant | MODIFIER | c.242-1676A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688138 | |||||||
chr4:140688245 | A | G | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-1783T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688245 | |||||||
chr4:140688414 | C | T | 27 | a0001c0001t0001g0012 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(24): Show |
intron_variant | MODIFIER | c.242-1952G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688414 | |||||||
chr4:140688496 | A | T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-2034T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688496 | |||||||
chr4:140688497 | T | G | 8 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.242-2035A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688497 | |||||||
chr4:140688608 | G | A | 2 | a0001c0005t0001g0160 a0001c0005t0009g0005 |
2 | HG02723.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.242-2146C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688608 | |||||||
chr4:140688624 | G | C | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.242-2162C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688624 | |||||||
chr4:140688630 | C | T | 2 | a0001c0004t0001g0229 a0001c0004t0002g0261 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242-2168G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688630 | |||||||
chr4:140688660 | C | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.242-2198G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688660 | |||||||
chr4:140688685 | C | A | 1 | a0001c0001t0001g0161 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.242-2223G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140688685 | |||||||
chr4:140689016 | C | T | 1 | a0001c0001t0002g0250 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.242-2554G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689016 | |||||||
chr4:140689019 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(209): Show |
212 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(209): Show |
intron_variant | MODIFIER | c.242-2557A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689019 | |||||||
chr4:140689041 | C | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-2579G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689041 | |||||||
chr4:140689135 | G | T | 99 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
99 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(96): Show |
intron_variant | MODIFIER | c.242-2673C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689135 | |||||||
chr4:140689206 | A | T | 1 | a0001c0007t0001g0230 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.242-2744T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689206 | |||||||
chr4:140689207 | T | C | 36 | a0001c0004t0001g0047 a0001c0004t0001g0105 a0001c0004t0001g0108 others(33): Show |
36 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.242-2745A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689207 | |||||||
chr4:140689240 | C | G | 1 | a0003c0019t0002g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.242-2778G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689240 | |||||||
chr4:140689315 | T | C | 12 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(9): Show |
12 | HG00639.hp1 HG01261.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.242-2853A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689315 | |||||||
chr4:140689336 | A | G | 5 | a0001c0004t0001g0225 a0001c0007t0001g0219 a0001c0007t0001g0220 others(2): Show |
5 | HG02083.hp2 NA18963.hp2 NA18989.hp2 others(2): Show |
intron_variant | MODIFIER | c.242-2874T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689336 | |||||||
chr4:140689376 | G | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-2914C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689376 | |||||||
chr4:140689393 | C | T | 2 | a0001c0004t0001g0153 a0001c0004t0001g0273 |
2 | HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.242-2931G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689393 | |||||||
chr4:140689401 | CTTCCCTT others(12): Show |
C | 5 | a0001c0004t0001g0087 a0001c0004t0001g0229 a0001c0004t0002g0261 others(2): Show |
5 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.242-2958_242-2940d others(21): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689401 | |||||||
chr4:140689455 | CCCCTT | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
219 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.242-2998_242-2994d others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689455 | |||||||
chr4:140689460 | T | TCCCTTCC others(137): Show |
2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.242-2999_242-2998i others(146): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689460 | |||||||
chr4:140689515 | CCT | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0161 others(50): Show |
53 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.242-3055_242-3054d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689515 | |||||||
chr4:140689603 | C | T | 1 | a0001c0001t0004g0293 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.242-3141G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689603 | |||||||
chr4:140689649 | CT | C | 33 | a0001c0002t0001g0138 a0001c0004t0001g0047 a0001c0004t0001g0105 others(30): Show |
33 | HG00558.hp2 HG00735.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.242-3188delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689649 | |||||||
chr4:140689650 | T | C | 3 | a0001c0004t0001g0120 a0001c0004t0001g0273 a0002c0009t0002g0046 |
3 | HG00408.hp2 HG02486.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.242-3188A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689650 | |||||||
chr4:140689674 | T | C | 218 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(215): Show |
218 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(215): Show |
intron_variant | MODIFIER | c.242-3212A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689674 | |||||||
chr4:140689754 | T | C | 21 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(18): Show |
21 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(18): Show |
intron_variant | MODIFIER | c.242-3292A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689754 | |||||||
chr4:140689854 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.242-3392A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140689854 | |||||||
chr4:140690072 | T | C | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.242-3610A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690072 | |||||||
chr4:140690136 | G | T | 2 | a0001c0003t0001g0072 a0001c0003t0001g0074 |
2 | HG02083.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.242-3674C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690136 | |||||||
chr4:140690171 | G | A | 195 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(192): Show |
195 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.242-3709C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690171 | |||||||
chr4:140690338 | A | G | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.242-3876T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690338 | |||||||
chr4:140690519 | T | C | 219 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(216): Show |
219 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.242-4057A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690519 | |||||||
chr4:140690672 | A | G | 1 | a0001c0003t0001g0254 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.242-4210T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690672 | |||||||
chr4:140690789 | C | T | 3 | a0001c0001t0001g0003 a0001c0002t0001g0245 a0001c0005t0001g0115 |
3 | HG02145.hp1 HG03209.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.242-4327G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690789 | |||||||
chr4:140690917 | C | T | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.242-4455G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140690917 | |||||||
chr4:140691113 | G | A | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.242-4651C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691113 | |||||||
chr4:140691131 | C | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.242-4669G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691131 | |||||||
chr4:140691154 | A | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.242-4692T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691154 | |||||||
chr4:140691253 | G | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.242-4791C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691253 | |||||||
chr4:140691352 | T | C | 18 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0162 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-4890A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691352 | |||||||
chr4:140691399 | C | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0062 a0001c0001t0001g0076 |
3 | HG00733.hp2 HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.242-4937G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691399 | |||||||
chr4:140691566 | C | T | 1 | a0001c0004t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.242-5104G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691566 | |||||||
chr4:140691623 | G | A | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.242-5161C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140691623 | |||||||
chr4:140692117 | G | C | 1 | a0001c0001t0002g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.242-5655C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692117 | |||||||
chr4:140692178 | T | C | 3 | a0001c0004t0001g0229 a0001c0004t0002g0261 a0001c0005t0001g0115 |
3 | HG02145.hp1 HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.242-5716A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692178 | |||||||
chr4:140692284 | G | A | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.242-5822C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692284 | |||||||
chr4:140692456 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.242-5994C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692456 | |||||||
chr4:140692563 | A | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0162 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-6101T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692563 | |||||||
chr4:140692677 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.242-6215G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692677 | |||||||
chr4:140692681 | C | T | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.242-6219G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692681 | |||||||
chr4:140692808 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.242-6346G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692808 | |||||||
chr4:140692843 | T | A | 136 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(133): Show |
137 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(134): Show |
intron_variant | MODIFIER | c.242-6381A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140692843 | |||||||
chr4:140693030 | A | T | 4 | a0001c0001t0001g0144 a0001c0004t0001g0087 a0001c0004t0005g0266 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-6568T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693030 | |||||||
chr4:140693051 | C | CA | 4 | a0001c0004t0001g0111 a0001c0004t0001g0124 a0001c0004t0001g0126 others(1): Show |
4 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.242-6590dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693051 | |||||||
chr4:140693130 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.242-6668G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693130 | |||||||
chr4:140693142 | T | C | 2 | a0001c0002t0001g0205 a0001c0002t0001g0233 |
2 | HG02523.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.242-6680A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693142 | |||||||
chr4:140693182 | C | T | 18 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(15): Show |
18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.242-6720G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693182 | |||||||
chr4:140693258 | A | T | 1 | a0001c0004t0001g0137 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.242-6796T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693258 | |||||||
chr4:140693290 | T | A | 1 | a0001c0007t0001g0239 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.242-6828A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693290 | |||||||
chr4:140693464 | C | T | 2 | a0001c0002t0001g0245 a0001c0021t0001g0265 |
2 | HG04184.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.242-7002G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693464 | |||||||
chr4:140693946 | A | T | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.242-7484T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140693946 | |||||||
chr4:140694058 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.241+7446T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694058 | |||||||
chr4:140694101 | A | G | 144 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(141): Show |
145 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.241+7403T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694101 | |||||||
chr4:140694155 | T | C | 1 | a0001c0002t0001g0233 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.241+7349A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694155 | |||||||
chr4:140694212 | C | T | 3 | a0001c0004t0001g0087 a0001c0004t0005g0266 a0001c0013t0011g0116 |
3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.241+7292G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694212 | |||||||
chr4:140694463 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0150 a0001c0001t0001g0152 others(3): Show |
6 | HG02572.hp1 HG02922.hp1 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.241+7041G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694463 | |||||||
chr4:140694570 | CA | C | 90 | a0001c0001t0003g0288 a0001c0002t0001g0051 a0001c0002t0001g0065 others(87): Show |
91 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(88): Show |
intron_variant | MODIFIER | c.241+6933delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694570 | |||||||
chr4:140694717 | G | A | 2 | a0001c0003t0001g0056 a0001c0003t0001g0079 |
2 | NA18991.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.241+6787C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694717 | |||||||
chr4:140694734 | A | G | 18 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0162 others(15): Show |
18 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+6770T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694734 | |||||||
chr4:140694796 | T | TA | 144 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(141): Show |
145 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(142): Show |
intron_variant | MODIFIER | c.241+6707_241+6708i others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694796 | |||||||
chr4:140694848 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+6656A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694848 | |||||||
chr4:140694879 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(4): Show |
7 | HG00544.hp1 HG01243.hp2 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.241+6625G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694879 | |||||||
chr4:140694930 | C | T | 16 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(13): Show |
16 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.241+6574G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694930 | |||||||
chr4:140694999 | C | T | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.241+6505G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140694999 | |||||||
chr4:140695013 | C | T | 4 | a0001c0001t0001g0024 a0001c0001t0003g0278 a0001c0001t0003g0279 others(1): Show |
4 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(1): Show |
intron_variant | MODIFIER | c.241+6491G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695013 | |||||||
chr4:140695018 | C | T | 3 | a0001c0004t0001g0087 a0001c0004t0005g0266 a0001c0013t0011g0116 |
3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.241+6486G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695018 | |||||||
chr4:140695134 | A | G | 18 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(15): Show |
18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+6370T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695134 | |||||||
chr4:140695340 | A | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0162 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.241+6164T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695340 | |||||||
chr4:140695664 | A | C | 1 | a0001c0001t0001g0195 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.241+5840T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695664 | |||||||
chr4:140695664 | A | G | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.241+5840T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695664 | |||||||
chr4:140695782 | T | G | 1 | a0001c0001t0003g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.241+5722A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695782 | |||||||
chr4:140695803 | A | G | 140 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(137): Show |
141 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(138): Show |
intron_variant | MODIFIER | c.241+5701T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695803 | |||||||
chr4:140695825 | C | T | 104 | a0001c0001t0001g0004 a0001c0001t0001g0161 a0001c0001t0001g0162 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.241+5679G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695825 | |||||||
chr4:140695840 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+5664G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695840 | |||||||
chr4:140695902 | A | G | 4 | a0001c0001t0001g0144 a0001c0004t0001g0087 a0001c0004t0005g0266 others(1): Show |
4 | HG02886.hp1 HG02896.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.241+5602T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695902 | |||||||
chr4:140695996 | T | A | 13 | a0001c0004t0001g0047 a0001c0004t0001g0120 a0001c0004t0001g0122 others(10): Show |
13 | HG00408.hp2 NA18964.hp1 NA18966.hp1 others(10): Show |
intron_variant | MODIFIER | c.241+5508A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140695996 | |||||||
chr4:140696025 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.241+5479T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696025 | |||||||
chr4:140696175 | GGGCCAGG others(6): Show |
G | 86 | a0001c0002t0001g0051 a0001c0002t0001g0065 a0001c0002t0001g0095 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.241+5316_241+5328d others(15): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696175 | |||||||
chr4:140696176 | G | A | 34 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(31): Show |
34 | HG00639.hp1 HG01192.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.241+5328C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696176 | |||||||
chr4:140696193 | CACGCCT | C | 86 | a0001c0002t0001g0051 a0001c0002t0001g0065 a0001c0002t0001g0095 others(83): Show |
87 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.241+5305_241+5310d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696193 | |||||||
chr4:140696286 | G | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(262): Show |
266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.241+5218C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696286 | |||||||
chr4:140696437 | C | G | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.241+5067G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696437 | |||||||
chr4:140696454 | T | G | 1 | a0001c0017t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.241+5050A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696454 | |||||||
chr4:140696455 | C | CA | 90 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.241+5048dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | |||||||
chr4:140696455 | C | CAA | 31 | a0001c0001t0001g0007 a0001c0001t0001g0015 a0001c0001t0001g0020 others(28): Show |
31 | HG00544.hp1 HG00544.hp2 HG00558.hp1 others(28): Show |
intron_variant | MODIFIER | c.241+5047_241+5048d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | |||||||
chr4:140696455 | CA | C | 17 | a0001c0001t0001g0162 a0001c0001t0001g0271 a0001c0001t0017g0297 others(14): Show |
17 | HG00609.hp2 HG00673.hp1 HG01069.hp1 others(14): Show |
intron_variant | MODIFIER | c.241+5048delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | |||||||
chr4:140696455 | CAA | C | 92 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00639.hp1 others(90): Show |
intron_variant | MODIFIER | c.241+5047_241+5048d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696455 | |||||||
chr4:140696498 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.241+5006A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696498 | |||||||
chr4:140696596 | G | C | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.241+4908C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696596 | |||||||
chr4:140696616 | C | T | 100 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
100 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(97): Show |
intron_variant | MODIFIER | c.241+4888G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696616 | |||||||
chr4:140696854 | G | A | 1 | a0001c0003t0001g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.241+4650C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696854 | |||||||
chr4:140696925 | A | T | 24 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(21): Show |
24 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.241+4579T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696925 | |||||||
chr4:140696944 | T | C | 1 | a0001c0008t0005g0242 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.241+4560A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696944 | |||||||
chr4:140696985 | T | C | 1 | a0001c0004t0001g0114 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.241+4519A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140696985 | |||||||
chr4:140697084 | A | G | 18 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(15): Show |
18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+4420T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697084 | |||||||
chr4:140697279 | G | A | 2 | a0001c0001t0001g0003 a0001c0005t0001g0115 |
2 | HG02145.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.241+4225C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697279 | |||||||
chr4:140697440 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241+4064G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697440 | |||||||
chr4:140697676 | A | C | 165 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(162): Show |
166 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(163): Show |
intron_variant | MODIFIER | c.241+3828T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697676 | |||||||
chr4:140697807 | A | G | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.241+3697T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140697807 | |||||||
chr4:140698166 | C | CT | 16 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(13): Show |
16 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.241+3337dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698166 | |||||||
chr4:140698278 | C | A | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.241+3226G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698278 | |||||||
chr4:140698379 | C | T | 98 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(95): Show |
98 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(95): Show |
intron_variant | MODIFIER | c.241+3125G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698379 | |||||||
chr4:140698380 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241+3124C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698380 | |||||||
chr4:140698489 | G | T | 1 | a0001c0001t0001g0077 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.241+3015C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698489 | |||||||
chr4:140698546 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.241+2958C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698546 | |||||||
chr4:140698653 | G | A | 32 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(29): Show |
32 | HG00639.hp1 HG01192.hp1 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.241+2851C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698653 | |||||||
chr4:140698714 | G | A | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
52 | HG00408.hp1 HG00544.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.241+2790C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698714 | |||||||
chr4:140698722 | AGTGAGAC others(14): Show |
A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.241+2761_241+2781d others(23): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698722 | |||||||
chr4:140698746 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.241+2758C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698746 | |||||||
chr4:140698746 | G | C | 79 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0012 others(76): Show |
79 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.241+2758C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698746 | |||||||
chr4:140698748 | G | A | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.241+2756C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698748 | |||||||
chr4:140698992 | G | A | 17 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.241+2512C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140698992 | |||||||
chr4:140699034 | T | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0061 a0001c0001t0001g0182 |
3 | HG03704.hp1 HG03710.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+2470A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699034 | |||||||
chr4:140699349 | A | G | 1 | a0001c0005t0001g0132 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.241+2155T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699349 | |||||||
chr4:140699435 | G | A | 3 | a0001c0001t0001g0110 a0001c0001t0001g0113 a0001c0001t0001g0163 |
3 | HG00741.hp2 HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.241+2069C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699435 | |||||||
chr4:140699533 | C | T | 14 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(11): Show |
14 | HG01106.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.241+1971G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699533 | |||||||
chr4:140699622 | G | T | 2 | a0001c0020t0001g0188 a0001c0021t0001g0265 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.241+1882C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699622 | |||||||
chr4:140699687 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+1817G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699687 | |||||||
chr4:140699762 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.241+1742C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699762 | |||||||
chr4:140699777 | T | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.241+1727A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699777 | |||||||
chr4:140699849 | G | T | 10 | a0001c0001t0001g0004 a0001c0004t0001g0087 a0001c0004t0001g0229 others(7): Show |
10 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.241+1655C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699849 | |||||||
chr4:140699933 | T | TA | 11 | a0001c0001t0001g0144 a0001c0005t0001g0129 a0001c0005t0001g0130 others(8): Show |
11 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.241+1570dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699933 | |||||||
chr4:140699971 | G | C | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.241+1533C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140699971 | |||||||
chr4:140700008 | C | T | 1 | a0001c0007t0001g0119 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.241+1496G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700008 | |||||||
chr4:140700021 | T | C | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.241+1483A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700021 | |||||||
chr4:140700085 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.241+1419G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700085 | |||||||
chr4:140700110 | A | G | 19 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0050 others(16): Show |
19 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.241+1394T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700110 | |||||||
chr4:140700151 | T | TA | 6 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.241+1352dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700151 | |||||||
chr4:140700163 | T | A | 2 | a0001c0001t0001g0218 a0001c0003t0001g0217 |
2 | HG02165.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.241+1341A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700163 | |||||||
chr4:140700214 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1290A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700214 | |||||||
chr4:140700215 | T | C | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1289A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700215 | |||||||
chr4:140700216 | G | A | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1288C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700216 | |||||||
chr4:140700220 | G | T | 2 | a0001c0001t0001g0060 a0001c0001t0001g0061 |
2 | HG01517.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.241+1284C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700220 | |||||||
chr4:140700225 | G | A | 148 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(145): Show |
149 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(146): Show |
intron_variant | MODIFIER | c.241+1279C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700225 | |||||||
chr4:140700310 | C | T | 2 | a0001c0002t0001g0210 a0001c0002t0001g0223 |
2 | HG03130.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.241+1194G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700310 | |||||||
chr4:140700404 | C | T | 1 | a0001c0010t0001g0191 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.241+1100G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700404 | |||||||
chr4:140700449 | C | CA | 15 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0166 others(12): Show |
15 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.241+1054dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700449 | |||||||
chr4:140700450 | A | C | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+1054T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700450 | |||||||
chr4:140700460 | C | A | 1 | a0001c0003t0001g0056 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.241+1044G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700460 | |||||||
chr4:140700474 | C | G | 179 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0024 others(176): Show |
180 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(177): Show |
intron_variant | MODIFIER | c.241+1030G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700474 | |||||||
chr4:140700531 | T | A | 3 | a0001c0001t0001g0144 a0001c0005t0001g0115 a0001c0008t0003g0276 |
3 | HG02145.hp1 HG03041.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.241+973A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700531 | |||||||
chr4:140700533 | T | C | 1 | a0001c0015t0002g0085 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.241+971A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700533 | |||||||
chr4:140700553 | C | A | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.241+951G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700553 | |||||||
chr4:140700608 | G | A | 2 | a0001c0005t0001g0115 a0001c0008t0003g0276 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.241+896C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700608 | |||||||
chr4:140700637 | A | G | 1 | a0001c0002t0001g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.241+867T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700637 | |||||||
chr4:140700815 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.241+689C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700815 | |||||||
chr4:140700821 | G | GA | 12 | a0001c0001t0001g0249 a0001c0003t0001g0056 a0001c0005t0001g0129 others(9): Show |
12 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.241+682dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700821 | |||||||
chr4:140700821 | GA | G | 18 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(15): Show |
18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.241+682delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700821 | |||||||
chr4:140700934 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0050 others(16): Show |
19 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.241+570C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700934 | |||||||
chr4:140700974 | C | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.241+530G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140700974 | |||||||
chr4:140701095 | C | T | 1 | a0001c0001t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.241+409G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701095 | |||||||
chr4:140701217 | A | G | 160 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(157): Show |
161 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(158): Show |
intron_variant | MODIFIER | c.241+287T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701217 | |||||||
chr4:140701239 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.241+265G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701239 | |||||||
chr4:140701281 | G | A | 2 | a0001c0001t0001g0045 a0001c0001t0001g0083 |
2 | HG00609.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.241+223C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701281 | |||||||
chr4:140701282 | G | A | 5 | a0001c0004t0001g0087 a0001c0004t0005g0266 a0001c0008t0001g0241 others(2): Show |
5 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.241+222C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701282 | |||||||
chr4:140701317 | G | C | 1 | a0001c0005t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.241+187C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 2/20 | chr4 | 140701317 | |||||||
chr4:140701665 | C | T | 14 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(11): Show |
14 | HG01106.hp2 HG02055.hp2 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-51G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701665 | |||||||
chr4:140701849 | CA | C | 102 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0162 others(99): Show |
103 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(100): Show |
intron_variant | MODIFIER | c.131-236delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701849 | |||||||
chr4:140701906 | G | C | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-292C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701906 | |||||||
chr4:140701909 | C | A | 8 | a0001c0001t0001g0162 a0001c0001t0001g0267 a0001c0001t0001g0271 others(5): Show |
8 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-295G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140701909 | |||||||
chr4:140702120 | C | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-506G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702120 | |||||||
chr4:140702187 | G | C | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-573C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702187 | |||||||
chr4:140702439 | G | C | 1 | a0001c0003t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.131-825C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702439 | |||||||
chr4:140702504 | G | A | 10 | a0001c0001t0001g0004 a0001c0004t0001g0087 a0001c0004t0001g0229 others(7): Show |
10 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-890C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702504 | |||||||
chr4:140702631 | T | C | 11 | a0001c0001t0001g0144 a0001c0005t0001g0129 a0001c0005t0001g0130 others(8): Show |
11 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-1017A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702631 | |||||||
chr4:140702636 | A | G | 271 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(268): Show |
272 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(269): Show |
intron_variant | MODIFIER | c.131-1022T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702636 | |||||||
chr4:140702773 | C | T | 93 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0185 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.131-1159G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702773 | |||||||
chr4:140702954 | T | G | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-1340A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140702954 | |||||||
chr4:140703025 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-1411A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703025 | |||||||
chr4:140703111 | G | A | 2 | a0001c0005t0001g0115 a0001c0008t0003g0276 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-1497C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703111 | |||||||
chr4:140703278 | C | G | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.131-1664G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703278 | |||||||
chr4:140703304 | T | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.131-1690A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703304 | |||||||
chr4:140703328 | G | A | 1 | a0001c0001t0003g0277 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.131-1714C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703328 | |||||||
chr4:140703378 | G | A | 3 | a0001c0001t0001g0024 a0001c0001t0003g0278 a0001c0001t0003g0282 |
3 | HG01257.hp1 HG01975.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.131-1764C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703378 | |||||||
chr4:140703399 | T | C | 1 | a0001c0002t0001g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-1785A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703399 | |||||||
chr4:140703433 | A | G | 1 | a0001c0001t0001g0057 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.131-1819T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703433 | |||||||
chr4:140703447 | C | T | 18 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0050 others(15): Show |
18 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(15): Show |
intron_variant | MODIFIER | c.131-1833G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703447 | |||||||
chr4:140703458 | A | C | 1 | a0001c0002t0001g0233 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.131-1844T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703458 | |||||||
chr4:140703490 | TGTGGA | T | 17 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-1881_131-1877d others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703490 | |||||||
chr4:140703519 | C | T | 149 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.131-1905G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703519 | |||||||
chr4:140703577 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.131-1963T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703577 | |||||||
chr4:140703581 | T | C | 17 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-1967A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703581 | |||||||
chr4:140703607 | T | G | 2 | a0001c0002t0001g0181 a0001c0002t0001g0243 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.131-1993A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703607 | |||||||
chr4:140703824 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-2210C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140703824 | |||||||
chr4:140704063 | G | A | 149 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(146): Show |
150 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(147): Show |
intron_variant | MODIFIER | c.131-2449C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704063 | |||||||
chr4:140704126 | G | A | 2 | a0001c0002t0001g0181 a0001c0002t0001g0243 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.131-2512C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704126 | |||||||
chr4:140704136 | A | C | 1 | a0001c0006t0001g0262 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.131-2522T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704136 | |||||||
chr4:140704142 | A | T | 1 | a0001c0006t0001g0262 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.131-2528T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704142 | |||||||
chr4:140704144 | T | A | 1 | a0001c0006t0001g0262 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.131-2530A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704144 | |||||||
chr4:140704207 | G | A | 2 | a0001c0002t0002g0232 a0001c0002t0003g0275 |
2 | HG01081.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.131-2593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704207 | |||||||
chr4:140704332 | C | T | 2 | a0001c0020t0001g0188 a0001c0021t0001g0265 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-2718G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704332 | |||||||
chr4:140704333 | G | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01517.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-2719C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704333 | |||||||
chr4:140704356 | A | G | 2 | a0001c0020t0001g0188 a0001c0021t0001g0265 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-2742T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704356 | |||||||
chr4:140704392 | C | G | 41 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(38): Show |
41 | HG01106.hp2 HG01192.hp1 HG01261.hp2 others(38): Show |
intron_variant | MODIFIER | c.131-2778G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704392 | |||||||
chr4:140704399 | T | TCAAA | 145 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(142): Show |
146 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(143): Show |
intron_variant | MODIFIER | c.131-2789_131-2786d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704399 | |||||||
chr4:140704435 | G | GA | 46 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0020 others(43): Show |
46 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.131-2822dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704435 | |||||||
chr4:140704435 | GA | G | 109 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0091 others(106): Show |
110 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(107): Show |
intron_variant | MODIFIER | c.131-2822delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704435 | |||||||
chr4:140704513 | C | G | 1 | a0001c0004t0001g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.131-2899G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704513 | |||||||
chr4:140704568 | G | C | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-2954C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704568 | |||||||
chr4:140704741 | A | G | 22 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(19): Show |
22 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-3127T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704741 | |||||||
chr4:140704743 | T | C | 11 | a0001c0001t0001g0144 a0001c0005t0001g0129 a0001c0005t0001g0130 others(8): Show |
11 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.131-3129A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704743 | |||||||
chr4:140704830 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(265): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.131-3216T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704830 | |||||||
chr4:140704846 | G | A | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-3232C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704846 | |||||||
chr4:140704941 | T | C | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.131-3327A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704941 | |||||||
chr4:140704950 | G | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-3336C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140704950 | |||||||
chr4:140705008 | A | G | 1 | a0001c0003t0001g0084 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.131-3394T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705008 | |||||||
chr4:140705343 | A | T | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-3729T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705343 | |||||||
chr4:140705503 | GGTGTGTG others(7): Show |
G | 1 | a0001c0002t0001g0051 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.131-3903_131-3890d others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705503 | |||||||
chr4:140705511 | CATGT | C | 3 | a0001c0005t0001g0132 a0001c0005t0001g0133 a0001c0005t0001g0134 |
3 | HG02630.hp1 NA19240.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.131-3901_131-3898d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705511 | |||||||
chr4:140705512 | ATG | A | 111 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0029 others(108): Show |
112 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.131-3900_131-3899d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705512 | |||||||
chr4:140705512 | ATGTG | A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0161 a0001c0001t0001g0177 others(19): Show |
22 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-3902_131-3899d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705512 | |||||||
chr4:140705512 | ATGTGTGT others(3): Show |
A | 22 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(19): Show |
22 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-3908_131-3899d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705512 | |||||||
chr4:140705522 | G | GTGTA | 17 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(14): Show |
17 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(14): Show |
intron_variant | MODIFIER | c.131-3909_131-3908i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705522 | |||||||
chr4:140705541 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.131-3927A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705541 | |||||||
chr4:140705953 | T | C | 3 | a0001c0004t0001g0087 a0001c0004t0005g0266 a0001c0013t0011g0116 |
3 | HG02886.hp1 HG02896.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.131-4339A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140705953 | |||||||
chr4:140706025 | A | C | 2 | a0001c0004t0001g0229 a0001c0004t0002g0261 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.131-4411T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706025 | |||||||
chr4:140706179 | C | T | 2 | a0001c0008t0001g0241 a0001c0008t0005g0242 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.131-4565G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706179 | |||||||
chr4:140706445 | C | T | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-4831G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706445 | |||||||
chr4:140706709 | T | A | 1 | a0001c0001t0003g0282 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.131-5095A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706709 | |||||||
chr4:140706903 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.131-5289T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706903 | |||||||
chr4:140706946 | C | T | 22 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(19): Show |
22 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.131-5332G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706946 | |||||||
chr4:140706947 | G | A | 10 | a0001c0001t0001g0004 a0001c0004t0001g0087 a0001c0004t0001g0229 others(7): Show |
10 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-5333C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140706947 | |||||||
chr4:140707018 | A | T | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.131-5404T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707018 | |||||||
chr4:140707050 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-5436T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707050 | |||||||
chr4:140707088 | C | G | 1 | a0001c0005t0001g0129 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.131-5474G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707088 | |||||||
chr4:140707128 | GT | G | 266 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(263): Show |
267 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(264): Show |
intron_variant | MODIFIER | c.131-5515delA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707128 | |||||||
chr4:140707568 | T | C | 28 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(25): Show |
28 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.131-5954A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707568 | |||||||
chr4:140707617 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-6003C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707617 | |||||||
chr4:140707680 | G | C | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-6066C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707680 | |||||||
chr4:140707751 | G | T | 42 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0091 others(39): Show |
42 | HG01192.hp1 HG01257.hp1 HG01884.hp2 others(39): Show |
intron_variant | MODIFIER | c.131-6137C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707751 | |||||||
chr4:140707761 | A | G | 103 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0162 others(100): Show |
104 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(101): Show |
intron_variant | MODIFIER | c.131-6147T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140707761 | |||||||
chr4:140708022 | A | G | 270 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(267): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.131-6408T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708022 | |||||||
chr4:140708475 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.131-6861G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708475 | |||||||
chr4:140708485 | T | C | 2 | a0001c0005t0001g0115 a0001c0008t0003g0276 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-6871A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708485 | |||||||
chr4:140708599 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-6985C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708599 | |||||||
chr4:140708616 | C | T | 2 | a0001c0001t0001g0057 a0001c0001t0001g0058 |
2 | HG03834.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.131-7002G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708616 | |||||||
chr4:140708631 | C | T | 6 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-7017G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708631 | |||||||
chr4:140708672 | C | T | 7 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0002g0103 others(4): Show |
7 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-7058G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708672 | |||||||
chr4:140708739 | T | C | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-7125A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708739 | |||||||
chr4:140708772 | T | A | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.131-7158A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708772 | |||||||
chr4:140708983 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-7369C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140708983 | |||||||
chr4:140709012 | G | A | 3 | a0001c0004t0001g0143 a0001c0020t0001g0188 a0001c0021t0001g0265 |
3 | HG03139.hp2 HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.131-7398C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709012 | |||||||
chr4:140709219 | A | ATC | 66 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(63): Show |
67 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.131-7607_131-7606d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709219 | A | ATCTC | 19 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0053 others(16): Show |
19 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.131-7609_131-7606d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709219 | A | ATCTCTC | 8 | a0001c0001t0001g0033 a0001c0001t0001g0057 a0001c0001t0001g0058 others(5): Show |
8 | HG02004.hp2 HG02155.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-7611_131-7606d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709219 | A | ATCTCTCT others(1): Show |
5 | a0001c0001t0001g0062 a0001c0003t0001g0009 a0001c0003t0001g0023 others(2): Show |
5 | HG00733.hp2 HG01167.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.131-7613_131-7606d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709219 | A | ATCTCTCT others(3): Show |
3 | a0001c0001t0001g0034 a0001c0001t0002g0244 a0001c0003t0001g0022 |
3 | HG01175.hp2 HG01943.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.131-7615_131-7606d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709219 | A | ATCTCTCT others(5): Show |
1 | a0001c0001t0001g0035 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.131-7617_131-7606d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709219 | ATC | A | 4 | a0001c0001t0001g0004 a0001c0001t0004g0294 a0001c0004t0001g0136 others(1): Show |
4 | HG00741.hp1 HG02280.hp1 HG02723.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-7607_131-7606d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709219 | |||||||
chr4:140709238 | TCTCTCTC others(5): Show |
T | 4 | a0001c0004t0001g0087 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG02886.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-7636_131-7625d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709238 | |||||||
chr4:140709240 | TCTCTCTC others(3): Show |
T | 2 | a0001c0004t0001g0229 a0001c0004t0002g0261 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.131-7636_131-7627d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709240 | |||||||
chr4:140709242 | TCTCTCTC others(3): Show |
T | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-7638_131-7629d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709242 | |||||||
chr4:140709244 | T | A | 8 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0151 others(5): Show |
8 | HG01192.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-7630A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | |||||||
chr4:140709244 | T | TCACA | 7 | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0154 others(4): Show |
7 | HG01884.hp2 HG02055.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-7631_131-7630i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | |||||||
chr4:140709244 | T | TCACACA | 3 | a0001c0001t0001g0091 a0001c0001t0001g0139 a0001c0001t0001g0162 |
3 | HG01891.hp1 HG02630.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.131-7631_131-7630i others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | |||||||
chr4:140709244 | TCTCTCA | T | 14 | a0001c0001t0001g0003 a0001c0001t0001g0024 a0001c0001t0001g0050 others(11): Show |
14 | HG01975.hp1 HG01978.hp2 HG02165.hp2 others(11): Show |
intron_variant | MODIFIER | c.131-7636_131-7631d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | |||||||
chr4:140709244 | TCTCTCAC others(5): Show |
T | 1 | a0001c0001t0001g0168 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.131-7642_131-7631d others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709244 | |||||||
chr4:140709246 | T | A | 23 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0139 others(20): Show |
23 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-7632A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709246 | |||||||
chr4:140709246 | T | TCACA | 7 | a0001c0001t0001g0093 a0001c0004t0001g0120 a0001c0004t0001g0122 others(4): Show |
7 | HG00408.hp2 HG02809.hp2 NA18964.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-7633_131-7632i others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709246 | |||||||
chr4:140709248 | T | A | 49 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(46): Show |
49 | HG00408.hp2 HG00558.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.131-7634A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCA | 3 | a0001c0001t0001g0271 a0001c0002t0015g0280 a0001c0004t0001g0143 |
3 | HG03139.hp2 HG04228.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.131-7636_131-7635d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCACACA | 3 | a0001c0001t0002g0270 a0001c0004t0001g0273 a0001c0006t0001g0258 |
3 | HG02486.hp1 HG02647.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.131-7640_131-7635d others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCACACAC others(3): Show |
3 | a0001c0001t0003g0287 a0001c0001t0003g0288 a0001c0020t0001g0188 |
3 | HG01070.hp2 HG01071.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.131-7644_131-7635d others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCACA | 5 | a0001c0001t0005g0096 a0001c0002t0001g0174 a0001c0002t0001g0216 others(2): Show |
5 | HG02145.hp2 HG02572.hp2 HG02735.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-7635_131-7634i others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCACAC others(3): Show |
1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-7635_131-7634i others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCAC others(3): Show |
2 | a0001c0002t0001g0196 a0001c0012t0008g0147 |
2 | HG01496.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.131-7635_131-7634i others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCAC others(5): Show |
2 | a0001c0001t0001g0267 a0001c0008t0001g0184 |
2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.131-7635_131-7634i others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCAC others(9): Show |
1 | a0001c0002t0001g0246 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.131-7635_131-7634i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCTC others(5): Show |
1 | a0001c0001t0001g0052 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.131-7635_131-7634i others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCTC others(9): Show |
1 | a0001c0002t0006g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.131-7635_131-7634i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCTC others(11): Show |
2 | a0001c0002t0001g0098 a0001c0002t0001g0100 |
2 | HG02622.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.131-7635_131-7634i others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCTC others(13): Show |
1 | a0001c0002t0001g0101 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.131-7635_131-7634i others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | T | TCTCTCTC others(9): Show |
1 | a0001c0002t0006g0099 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.131-7635_131-7634i others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | TCA | T | 44 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0015 others(41): Show |
44 | HG00099.hp1 HG00408.hp1 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.131-7636_131-7635d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | TCACA | T | 3 | a0001c0001t0001g0045 a0001c0008t0003g0276 a0001c0016t0012g0272 |
3 | HG00609.hp1 HG02559.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-7638_131-7635d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | TCACACAC others(1): Show |
T | 8 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(5): Show |
8 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-7642_131-7635d others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709248 | TCACACAC others(7): Show |
T | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-7648_131-7635d others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709248 | |||||||
chr4:140709250 | A | T | 83 | a0001c0001t0001g0008 a0001c0001t0001g0010 a0001c0001t0001g0011 others(80): Show |
84 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(81): Show |
intron_variant | MODIFIER | c.131-7636T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709250 | |||||||
chr4:140709252 | A | T | 114 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
intron_variant | MODIFIER | c.131-7638T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709252 | |||||||
chr4:140709254 | A | T | 62 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(59): Show |
62 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.131-7640T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709254 | |||||||
chr4:140709256 | A | T | 52 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(49): Show |
52 | HG00099.hp1 HG00408.hp1 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.131-7642T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709256 | |||||||
chr4:140709258 | A | T | 2 | a0001c0001t0001g0064 a0001c0003t0001g0086 |
2 | HG03491.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.131-7644T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709258 | |||||||
chr4:140709260 | A | T | 1 | a0001c0003t0001g0086 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.131-7646T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709260 | |||||||
chr4:140709283 | C | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-7669G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709283 | |||||||
chr4:140709288 | A | C | 2 | a0001c0001t0003g0286 a0001c0002t0002g0232 |
2 | HG01975.hp2 HG02165.hp2 |
intron_variant | MODIFIER | c.131-7674T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709288 | |||||||
chr4:140709308 | G | A | 1 | a0001c0006t0001g0264 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.131-7694C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709308 | |||||||
chr4:140709414 | G | A | 1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-7800C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709414 | |||||||
chr4:140709454 | T | C | 24 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(21): Show |
24 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.131-7840A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709454 | |||||||
chr4:140709502 | T | TA | 78 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(75): Show |
78 | HG00639.hp1 HG01106.hp2 HG01192.hp1 others(75): Show |
intron_variant | MODIFIER | c.131-7889dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709502 | |||||||
chr4:140709502 | TA | T | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.131-7889delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709502 | |||||||
chr4:140709664 | A | G | 76 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(73): Show |
76 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(73): Show |
intron_variant | MODIFIER | c.131-8050T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709664 | |||||||
chr4:140709706 | C | T | 1 | a0001c0001t0002g0014 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.131-8092G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709706 | |||||||
chr4:140709807 | A | G | 1 | a0001c0001t0004g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.131-8193T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709807 | |||||||
chr4:140709874 | T | A | 1 | a0001c0010t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.131-8260A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709874 | |||||||
chr4:140709901 | G | T | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.131-8287C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140709901 | |||||||
chr4:140710104 | T | G | 2 | a0001c0001t0014g0284 a0001c0003t0003g0285 |
2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.131-8490A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710104 | |||||||
chr4:140710202 | G | A | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-8588C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710202 | |||||||
chr4:140710474 | C | T | 87 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(84): Show |
87 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(84): Show |
intron_variant | MODIFIER | c.131-8860G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710474 | |||||||
chr4:140710563 | A | G | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-8949T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710563 | |||||||
chr4:140710576 | C | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-8962G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710576 | |||||||
chr4:140710619 | G | A | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131-9005C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710619 | |||||||
chr4:140710651 | C | G | 10 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0001g0132 others(7): Show |
10 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-9037G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140710651 | |||||||
chr4:140711009 | G | A | 263 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(260): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.131-9395C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711009 | |||||||
chr4:140711150 | C | T | 79 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(76): Show |
79 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(76): Show |
intron_variant | MODIFIER | c.131-9536G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711150 | |||||||
chr4:140711157 | T | G | 27 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(24): Show |
27 | HG01257.hp1 HG01261.hp2 HG01975.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-9543A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711157 | |||||||
chr4:140711349 | T | C | 1 | a0001c0008t0003g0276 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.131-9735A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711349 | |||||||
chr4:140711385 | C | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0002g0092 |
3 | HG02615.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.131-9771G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711385 | |||||||
chr4:140711434 | G | C | 12 | a0001c0001t0001g0004 a0001c0001t0002g0274 a0001c0004t0001g0087 others(9): Show |
12 | HG01261.hp2 HG02280.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-9820C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711434 | |||||||
chr4:140711470 | C | G | 24 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(21): Show |
24 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(21): Show |
intron_variant | MODIFIER | c.131-9856G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711470 | |||||||
chr4:140711536 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(25): Show |
28 | HG01257.hp1 HG01261.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-9922G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711536 | |||||||
chr4:140711550 | C | A | 28 | a0001c0001t0001g0004 a0001c0001t0001g0024 a0001c0001t0001g0050 others(25): Show |
28 | HG01257.hp1 HG01261.hp2 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.131-9936G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711550 | |||||||
chr4:140711791 | C | T | 1 | a0001c0002t0001g0190 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.131-10177G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711791 | |||||||
chr4:140711819 | C | T | 15 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(12): Show |
15 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.131-10205G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711819 | |||||||
chr4:140711857 | G | A | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-10243C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711857 | |||||||
chr4:140711939 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-10325T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711939 | |||||||
chr4:140711947 | A | G | 3 | a0001c0002t0001g0174 a0001c0002t0003g0281 a0001c0002t0003g0290 |
3 | HG01074.hp2 HG02559.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.131-10333T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140711947 | |||||||
chr4:140712080 | C | T | 22 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(19): Show |
22 | HG00639.hp1 HG01106.hp2 HG01361.hp2 others(19): Show |
intron_variant | MODIFIER | c.131-10466G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712080 | |||||||
chr4:140712150 | G | A | 1 | a0001c0005t0002g0131 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.131-10536C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712150 | |||||||
chr4:140712153 | CATATCTA others(289): Show |
C | 15 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0140 others(12): Show |
15 | HG01257.hp1 HG01975.hp1 HG01978.hp2 others(12): Show |
intron_variant | MODIFIER | c.131-10835_131-1054 others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712153 | |||||||
chr4:140712291 | T | C | 23 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(20): Show |
23 | HG01192.hp1 HG01884.hp2 HG01891.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-10677A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712291 | |||||||
chr4:140712298 | A | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-10684T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712298 | |||||||
chr4:140712381 | C | A | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-10767G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712381 | |||||||
chr4:140712438 | T | A | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-10824A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712438 | |||||||
chr4:140712449 | A | AAATATAT others(40): Show |
1 | a0001c0007t0001g0219 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.131-10836_131-1083 others(51): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(3): Show |
2 | a0001c0001t0001g0003 a0001c0001t0001g0267 |
2 | HG02451.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.131-10845_131-1083 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(5): Show |
30 | a0001c0001t0001g0007 a0001c0001t0001g0033 a0001c0001t0001g0034 others(27): Show |
30 | HG00140.hp1 HG00621.hp1 HG00733.hp2 others(27): Show |
intron_variant | MODIFIER | c.131-10847_131-1083 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(7): Show |
48 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(45): Show |
48 | HG00099.hp1 HG00408.hp1 HG00423.hp1 others(45): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(9): Show |
4 | a0001c0001t0001g0016 a0001c0001t0001g0144 a0001c0001t0002g0014 others(1): Show |
4 | NA18953.hp2 NA18981.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(11): Show |
18 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(15): Show |
18 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(13): Show |
6 | a0001c0001t0001g0155 a0001c0001t0001g0164 a0001c0001t0002g0090 others(3): Show |
6 | HG01192.hp1 HG02886.hp1 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(24): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(15): Show |
7 | a0001c0001t0001g0156 a0001c0001t0002g0274 a0001c0002t0001g0190 others(4): Show |
7 | HG02615.hp1 HG02965.hp2 HG03453.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(26): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(41): Show |
1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.131-10836_131-1083 others(52): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(17): Show |
1 | a0001c0002t0006g0165 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.131-10836_131-1083 others(28): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(19): Show |
4 | a0001c0001t0001g0208 a0001c0001t0003g0287 a0001c0001t0003g0288 others(1): Show |
4 | HG01070.hp2 HG01071.hp2 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(30): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(21): Show |
12 | a0001c0001t0001g0161 a0001c0002t0001g0174 a0001c0002t0001g0189 others(9): Show |
12 | HG00099.hp2 HG00140.hp2 HG01167.hp1 others(9): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(23): Show |
19 | a0001c0001t0001g0204 a0001c0001t0006g0142 a0001c0001t0014g0284 others(16): Show |
19 | HG01169.hp1 HG01884.hp1 HG02145.hp2 others(16): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(34): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(25): Show |
35 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0170 others(32): Show |
36 | HG00609.hp2 HG00639.hp1 HG01081.hp1 others(33): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(36): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(27): Show |
27 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0218 others(24): Show |
27 | HG00639.hp2 HG00673.hp1 HG00733.hp1 others(24): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(38): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(29): Show |
18 | a0001c0001t0001g0162 a0001c0001t0001g0185 a0001c0001t0001g0199 others(15): Show |
18 | HG01069.hp2 HG01346.hp2 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(40): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(31): Show |
3 | a0001c0001t0001g0029 a0001c0003t0001g0217 a0001c0008t0005g0242 |
3 | HG01261.hp2 HG02165.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.131-10836_131-1083 others(42): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(33): Show |
10 | a0001c0001t0001g0212 a0001c0002t0001g0112 a0001c0002t0001g0211 others(7): Show |
10 | HG01891.hp2 HG02300.hp2 HG03139.hp2 others(7): Show |
intron_variant | MODIFIER | c.131-10836_131-1083 others(44): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(35): Show |
2 | a0001c0007t0001g0220 a0001c0007t0001g0230 |
2 | NA18963.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.131-10836_131-1083 others(46): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | AATATATA others(39): Show |
1 | a0001c0002t0001g0222 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.131-10836_131-1083 others(50): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712449 | A | ATTATATA others(25): Show |
2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-10836_131-1083 others(36): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712449 | |||||||
chr4:140712470 | C | T | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.131-10856G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712470 | |||||||
chr4:140712513 | C | T | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-10899G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712513 | |||||||
chr4:140712674 | G | A | 1 | a0001c0001t0003g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.131-11060C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712674 | |||||||
chr4:140712748 | A | AATAG | 18 | a0001c0001t0001g0094 a0001c0001t0001g0195 a0001c0001t0001g0271 others(15): Show |
18 | HG00140.hp1 HG00642.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-11138_131-1113 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | |||||||
chr4:140712748 | A | AATAGATA others(1): Show |
86 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0012 others(83): Show |
86 | HG00099.hp1 HG00423.hp1 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.131-11142_131-1113 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | |||||||
chr4:140712748 | A | AATAGATA others(5): Show |
55 | a0001c0001t0001g0004 a0001c0001t0001g0007 a0001c0001t0001g0008 others(52): Show |
55 | HG00408.hp1 HG00544.hp2 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.131-11146_131-1113 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | |||||||
chr4:140712748 | A | AATAGATA others(9): Show |
1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.131-11150_131-1113 others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | |||||||
chr4:140712748 | AATAG | A | 12 | a0001c0001t0005g0096 a0001c0002t0001g0098 a0001c0002t0001g0100 others(9): Show |
12 | HG00735.hp1 HG01884.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-11138_131-1113 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | |||||||
chr4:140712748 | AATAGATA others(1): Show |
A | 94 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0117 others(91): Show |
95 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(92): Show |
intron_variant | MODIFIER | c.131-11142_131-1113 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712748 | |||||||
chr4:140712932 | C | G | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-11318G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140712932 | |||||||
chr4:140713150 | C | G | 81 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(78): Show |
81 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(78): Show |
intron_variant | MODIFIER | c.131-11536G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713150 | |||||||
chr4:140713294 | T | C | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.131-11680A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713294 | |||||||
chr4:140713303 | C | T | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-11689G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713303 | |||||||
chr4:140713390 | G | A | 1 | a0001c0001t0004g0294 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.131-11776C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713390 | |||||||
chr4:140713749 | T | TA | 133 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(130): Show |
134 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(131): Show |
intron_variant | MODIFIER | c.131-12136dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | |||||||
chr4:140713749 | T | TAA | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-12137_131-1213 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | |||||||
chr4:140713749 | T | TAAA | 26 | a0001c0001t0001g0050 a0001c0001t0001g0140 a0001c0001t0001g0141 others(23): Show |
26 | HG01106.hp2 HG02055.hp2 HG02145.hp1 others(23): Show |
intron_variant | MODIFIER | c.131-12138_131-1213 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | |||||||
chr4:140713749 | T | TAAAA | 8 | a0001c0001t0001g0004 a0001c0001t0002g0274 a0001c0004t0001g0087 others(5): Show |
8 | HG01261.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-12139_131-1213 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713749 | |||||||
chr4:140713759 | A | AAAC | 7 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0002g0103 others(4): Show |
7 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-12148_131-1214 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713759 | |||||||
chr4:140713843 | T | C | 2 | a0001c0005t0001g0115 a0001c0008t0003g0276 |
2 | HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.131-12229A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713843 | |||||||
chr4:140713846 | A | G | 3 | a0001c0004t0001g0105 a0001c0004t0001g0108 a0001c0007t0007g0107 |
3 | HG00558.hp2 NA18981.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.131-12232T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713846 | |||||||
chr4:140713939 | A | T | 1 | a0001c0003t0003g0285 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.131-12325T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140713939 | |||||||
chr4:140714167 | C | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.131-12553G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714167 | |||||||
chr4:140714179 | T | C | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.131-12565A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714179 | |||||||
chr4:140714224 | T | C | 1 | a0001c0002t0001g0231 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.131-12610A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714224 | |||||||
chr4:140714251 | C | T | 7 | a0001c0001t0002g0183 a0001c0002t0001g0196 a0001c0002t0001g0246 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-12637G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714251 | |||||||
chr4:140714311 | G | T | 8 | a0001c0001t0001g0004 a0001c0001t0002g0274 a0001c0004t0001g0087 others(5): Show |
8 | HG01261.hp2 HG02280.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-12697C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714311 | |||||||
chr4:140714406 | C | T | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.131-12792G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714406 | |||||||
chr4:140714445 | C | T | 1 | a0001c0002t0001g0202 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.131-12831G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714445 | |||||||
chr4:140714450 | G | T | 104 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0117 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.131-12836C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714450 | |||||||
chr4:140714493 | T | G | 96 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(93): Show |
96 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.131-12879A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714493 | |||||||
chr4:140714700 | T | C | 7 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0002g0103 others(4): Show |
7 | HG00639.hp1 HG01361.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-13086A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714700 | |||||||
chr4:140714778 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131-13164C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714778 | |||||||
chr4:140714833 | G | C | 10 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(7): Show |
10 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.131-13219C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140714833 | |||||||
chr4:140715103 | G | C | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.131-13489C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715103 | |||||||
chr4:140715167 | C | T | 1 | a0001c0017t0001g0159 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.131-13553G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715167 | |||||||
chr4:140715257 | C | G | 90 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(87): Show |
90 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.131-13643G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715257 | |||||||
chr4:140715269 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-13655G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715269 | |||||||
chr4:140715496 | C | T | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-13882G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715496 | |||||||
chr4:140715607 | A | G | 6 | a0001c0004t0001g0225 a0001c0007t0001g0219 a0001c0007t0001g0220 others(3): Show |
6 | HG02083.hp2 NA18963.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-13993T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715607 | |||||||
chr4:140715609 | T | G | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131-13995A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715609 | |||||||
chr4:140715611 | T | C | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.131-13997A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715611 | |||||||
chr4:140715778 | A | C | 1 | a0001c0001t0014g0284 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.131-14164T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140715778 | |||||||
chr4:140716016 | C | T | 1 | a0001c0004t0001g0105 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.131-14402G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716016 | |||||||
chr4:140716121 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-14507A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716121 | |||||||
chr4:140716130 | C | A | 6 | a0001c0004t0001g0225 a0001c0007t0001g0219 a0001c0007t0001g0220 others(3): Show |
6 | HG02083.hp2 NA18963.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.131-14516G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716130 | |||||||
chr4:140716324 | C | CAAAAAGT others(312): Show |
1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-14711_131-1471 others(323): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716324 | |||||||
chr4:140716507 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.131-14893T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716507 | |||||||
chr4:140716574 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.131-14960A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716574 | |||||||
chr4:140716600 | T | C | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-14986A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716600 | |||||||
chr4:140716623 | C | T | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.131-15009G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716623 | |||||||
chr4:140716921 | T | TA | 101 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0010 others(98): Show |
101 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.131-15308dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140716921 | |||||||
chr4:140717014 | C | T | 12 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(9): Show |
12 | HG01257.hp1 HG01975.hp1 HG02165.hp2 others(9): Show |
intron_variant | MODIFIER | c.131-15400G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717014 | |||||||
chr4:140717082 | A | G | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-15468T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717082 | |||||||
chr4:140717271 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.131-15657C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717271 | |||||||
chr4:140717429 | T | C | 1 | a0001c0002t0001g0214 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.131-15815A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717429 | |||||||
chr4:140717586 | G | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-15972C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717586 | |||||||
chr4:140717608 | T | C | 132 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-15994A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717608 | |||||||
chr4:140717636 | T | G | 8 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0002g0274 others(5): Show |
8 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.131-16022A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717636 | |||||||
chr4:140717839 | C | T | 1 | a0001c0001t0002g0244 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.131-16225G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717839 | |||||||
chr4:140717918 | T | C | 262 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.131-16304A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140717918 | |||||||
chr4:140718247 | G | GA | 191 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.131-16634dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718247 | |||||||
chr4:140718304 | C | T | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-16690G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718304 | |||||||
chr4:140718345 | T | G | 2 | a0001c0005t0001g0146 a0001c0005t0001g0158 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.131-16731A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718345 | |||||||
chr4:140718449 | A | G | 1 | a0001c0002t0002g0221 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.131-16835T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718449 | |||||||
chr4:140718489 | C | A | 1 | a0001c0002t0015g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-16875G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718489 | |||||||
chr4:140718560 | C | T | 132 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(129): Show |
133 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(130): Show |
intron_variant | MODIFIER | c.131-16946G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718560 | |||||||
chr4:140718633 | C | T | 7 | a0001c0001t0001g0162 a0001c0001t0001g0271 a0001c0001t0002g0270 others(4): Show |
7 | HG01070.hp2 HG01071.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-17019G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718633 | |||||||
chr4:140718637 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-17023A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718637 | |||||||
chr4:140718936 | T | A | 4 | a0001c0001t0014g0284 a0001c0003t0003g0285 a0001c0008t0003g0276 others(1): Show |
4 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-17322A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140718936 | |||||||
chr4:140719115 | A | AAAAT | 23 | a0001c0001t0001g0145 a0001c0001t0001g0148 a0001c0001t0001g0149 others(20): Show |
23 | HG00673.hp1 HG01106.hp2 HG01361.hp1 others(20): Show |
intron_variant | MODIFIER | c.131-17505_131-1750 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719115 | A | AAAATAAA others(1): Show |
7 | a0001c0001t0001g0004 a0001c0001t0001g0123 a0001c0001t0001g0166 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG01496.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-17509_131-1750 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719115 | AAAAT | A | 38 | a0001c0001t0001g0008 a0001c0001t0001g0011 a0001c0001t0001g0012 others(35): Show |
38 | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(35): Show |
intron_variant | MODIFIER | c.131-17505_131-1750 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719115 | AAAATAAA others(1): Show |
A | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-17509_131-1750 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719115 | AAAATAAA others(5): Show |
A | 3 | a0001c0006t0001g0206 a0001c0008t0001g0186 a0001c0008t0002g0187 |
3 | HG02647.hp2 HG03139.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.131-17513_131-1750 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719115 | AAAATAAA others(9): Show |
A | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-17517_131-1750 others(20): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719115 | AAAATAAA others(21): Show |
A | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.131-17529_131-1750 others(32): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719115 | |||||||
chr4:140719139 | T | C | 2 | a0001c0002t0001g0227 a0001c0006t0001g0258 |
2 | NA18967.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.131-17525A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719139 | |||||||
chr4:140719161 | A | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0192 |
2 | HG00544.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.131-17547T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719161 | |||||||
chr4:140719359 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.131-17745G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719359 | |||||||
chr4:140719419 | G | A | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.131-17805C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719419 | |||||||
chr4:140719590 | T | C | 1 | a0001c0001t0002g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.131-17976A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719590 | |||||||
chr4:140719685 | T | C | 3 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0004g0292 |
3 | NA18948.hp2 NA19074.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.131-18071A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140719685 | |||||||
chr4:140720070 | T | C | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.131-18456A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720070 | |||||||
chr4:140720094 | T | G | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.131-18480A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720094 | |||||||
chr4:140720283 | A | G | 14 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(11): Show |
14 | HG00733.hp1 HG01257.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.131-18669T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720283 | |||||||
chr4:140720375 | A | C | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-18761T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720375 | |||||||
chr4:140720577 | G | C | 2 | a0001c0001t0001g0140 a0001c0001t0001g0141 |
2 | HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.131-18963C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720577 | |||||||
chr4:140720699 | G | C | 84 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(81): Show |
84 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(81): Show |
intron_variant | MODIFIER | c.131-19085C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720699 | |||||||
chr4:140720787 | C | G | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.131-19173G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720787 | |||||||
chr4:140720908 | T | C | 1 | a0001c0002t0001g0215 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.131-19294A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140720908 | |||||||
chr4:140721049 | G | A | 3 | a0001c0002t0001g0216 a0001c0002t0001g0227 a0001c0006t0001g0258 |
3 | NA18967.hp2 NA18975.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.131-19435C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721049 | |||||||
chr4:140721062 | C | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(239): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.131-19448G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721062 | |||||||
chr4:140721272 | A | G | 1 | a0001c0001t0003g0278 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.131-19658T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721272 | |||||||
chr4:140721692 | C | T | 130 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.131-20078G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721692 | |||||||
chr4:140721765 | C | T | 130 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0091 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.131-20151G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721765 | |||||||
chr4:140721966 | C | T | 7 | a0001c0001t0002g0183 a0001c0002t0001g0196 a0001c0002t0001g0246 others(4): Show |
7 | HG01243.hp1 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.131-20352G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140721966 | |||||||
chr4:140722005 | T | C | 3 | a0001c0002t0003g0281 a0001c0002t0003g0283 a0001c0002t0003g0290 |
3 | HG01074.hp2 HG01361.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.131-20391A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722005 | |||||||
chr4:140722096 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-20482A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722096 | |||||||
chr4:140722273 | G | GA | 7 | a0001c0001t0001g0135 a0001c0001t0002g0274 a0001c0002t0002g0088 others(4): Show |
7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-20660dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722273 | |||||||
chr4:140722341 | C | T | 21 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(18): Show |
21 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-20727G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722341 | |||||||
chr4:140722518 | G | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.131-20904C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722518 | |||||||
chr4:140722534 | T | C | 5 | a0001c0001t0002g0183 a0001c0008t0001g0184 a0001c0008t0001g0186 others(2): Show |
5 | HG02451.hp2 HG02647.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.131-20920A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722534 | |||||||
chr4:140722591 | T | C | 1 | a0001c0003t0001g0069 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.131-20977A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722591 | |||||||
chr4:140722657 | G | T | 1 | a0001c0005t0002g0128 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.131-21043C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722657 | |||||||
chr4:140722866 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-21252C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722866 | |||||||
chr4:140722888 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.131-21274A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722888 | |||||||
chr4:140722906 | C | T | 4 | a0001c0001t0014g0284 a0001c0003t0003g0285 a0001c0004t0001g0087 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-21292G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140722906 | |||||||
chr4:140723218 | C | T | 3 | a0001c0001t0001g0144 a0001c0001t0001g0162 a0001c0001t0017g0297 |
3 | HG02258.hp2 HG03486.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.131-21604G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723218 | |||||||
chr4:140723220 | T | C | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-21606A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723220 | |||||||
chr4:140723326 | C | A | 1 | a0001c0001t0001g0177 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.131-21712G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723326 | |||||||
chr4:140723375 | G | A | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.131-21761C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723375 | |||||||
chr4:140723754 | T | G | 4 | a0001c0004t0005g0266 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-22140A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723754 | |||||||
chr4:140723900 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-22286C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140723900 | |||||||
chr4:140724154 | G | A | 18 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(15): Show |
18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-22540C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724154 | |||||||
chr4:140724497 | C | T | 1 | a0001c0001t0001g0050 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.131-22883G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724497 | |||||||
chr4:140724530 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.131-22916G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724530 | |||||||
chr4:140724640 | GA | G | 6 | a0001c0001t0001g0004 a0001c0001t0001g0045 a0001c0001t0001g0083 others(3): Show |
6 | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23027delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724640 | |||||||
chr4:140724716 | T | C | 1 | a0001c0007t0001g0239 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.131-23102A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724716 | |||||||
chr4:140724802 | A | T | 1 | a0003c0019t0002g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.131-23188T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140724802 | |||||||
chr4:140725069 | C | T | 1 | a0001c0003t0001g0041 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.131-23455G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725069 | |||||||
chr4:140725123 | C | T | 2 | a0001c0002t0003g0281 a0001c0002t0003g0290 |
2 | HG01074.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.131-23509G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725123 | |||||||
chr4:140725179 | T | A | 18 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(15): Show |
18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-23565A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725179 | |||||||
chr4:140725284 | G | A | 6 | a0001c0001t0001g0204 a0001c0001t0001g0249 a0001c0002t0001g0190 others(3): Show |
6 | NA18941.hp2 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.131-23670C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725284 | |||||||
chr4:140725446 | T | G | 4 | a0001c0001t0002g0044 a0001c0001t0010g0055 a0001c0003t0001g0056 others(1): Show |
4 | HG02155.hp1 NA18991.hp1 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-23832A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725446 | |||||||
chr4:140725688 | T | G | 21 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(18): Show |
21 | HG01884.hp2 HG01891.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.131-24074A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725688 | |||||||
chr4:140725718 | T | C | 4 | a0001c0005t0001g0129 a0001c0005t0001g0130 a0001c0005t0002g0128 others(1): Show |
4 | HG00639.hp1 HG02300.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-24104A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140725718 | |||||||
chr4:140726106 | T | C | 8 | a0001c0003t0001g0097 a0001c0005t0001g0129 a0001c0005t0001g0130 others(5): Show |
8 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.131-24492A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726106 | |||||||
chr4:140726247 | C | T | 1 | a0003c0019t0002g0125 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.131-24633G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726247 | |||||||
chr4:140726302 | T | A | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-24688A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726302 | |||||||
chr4:140726306 | A | T | 4 | a0001c0001t0001g0003 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02630.hp2 HG03209.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.131-24692T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726306 | |||||||
chr4:140726366 | T | C | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.131-24752A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726366 | |||||||
chr4:140726513 | A | C | 2 | a0001c0002t0001g0138 a0001c0004t0001g0137 |
2 | HG01928.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.131-24899T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726513 | |||||||
chr4:140726574 | C | A | 2 | a0001c0001t0001g0093 a0001c0001t0001g0094 |
2 | HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.131-24960G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726574 | |||||||
chr4:140726724 | C | T | 1 | a0001c0003t0001g0031 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.131-25110G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726724 | |||||||
chr4:140726725 | G | A | 2 | a0001c0001t0001g0053 a0001c0001t0001g0054 |
2 | HG01257.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.131-25111C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726725 | |||||||
chr4:140726735 | G | T | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.131-25121C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726735 | |||||||
chr4:140726946 | C | T | 18 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(15): Show |
18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.131-25332G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140726946 | |||||||
chr4:140727130 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.131-25516A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727130 | |||||||
chr4:140727291 | C | A | 4 | a0001c0002t0001g0245 a0001c0002t0001g0268 a0001c0002t0001g0269 others(1): Show |
4 | HG02559.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-25677G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727291 | |||||||
chr4:140727541 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.131-25927G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727541 | |||||||
chr4:140727739 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.131-26125A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727739 | |||||||
chr4:140727789 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.131-26175G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727789 | |||||||
chr4:140727832 | A | G | 1 | a0001c0002t0015g0280 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.131-26218T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140727832 | |||||||
chr4:140728280 | A | C | 2 | a0001c0002t0001g0197 a0001c0002t0001g0247 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.131-26666T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728280 | |||||||
chr4:140728323 | T | C | 7 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0004t0005g0266 others(4): Show |
7 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.131-26709A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728323 | |||||||
chr4:140728401 | TA | T | 138 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(135): Show |
139 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.131-26788delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728401 | |||||||
chr4:140728493 | T | C | 1 | a0001c0004t0001g0169 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.131-26879A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728493 | |||||||
chr4:140728619 | G | C | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.131-27005C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728619 | |||||||
chr4:140728701 | C | T | 4 | a0001c0004t0005g0266 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG02559.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.131-27087G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140728701 | |||||||
chr4:140729091 | T | C | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.130+26825A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729091 | |||||||
chr4:140729117 | C | T | 18 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(15): Show |
18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+26799G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729117 | |||||||
chr4:140729122 | C | T | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.130+26794G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729122 | |||||||
chr4:140729131 | C | A | 2 | a0001c0002t0001g0181 a0001c0002t0001g0243 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.130+26785G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729131 | |||||||
chr4:140729272 | T | C | 1 | a0001c0001t0002g0244 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+26644A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729272 | |||||||
chr4:140729418 | C | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+26498G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729418 | |||||||
chr4:140729436 | T | A | 12 | a0001c0001t0001g0218 a0001c0002t0001g0224 a0001c0003t0001g0217 others(9): Show |
12 | HG02083.hp2 HG02165.hp1 HG02523.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+26480A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729436 | |||||||
chr4:140729442 | C | T | 3 | a0001c0002t0001g0245 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02896.hp1 HG02897.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.130+26474G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729442 | |||||||
chr4:140729446 | A | G | 7 | a0001c0001t0001g0135 a0001c0001t0002g0274 a0001c0002t0002g0088 others(4): Show |
7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+26470T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729446 | |||||||
chr4:140729487 | C | G | 3 | a0001c0001t0001g0195 a0001c0002t0001g0065 a0001c0003t0007g0013 |
3 | NA18964.hp2 NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.130+26429G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729487 | |||||||
chr4:140729647 | G | A | 1 | a0001c0001t0003g0279 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.130+26269C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729647 | |||||||
chr4:140729693 | G | A | 1 | a0001c0008t0002g0187 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.130+26223C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729693 | |||||||
chr4:140729697 | G | A | 2 | a0001c0008t0001g0180 a0001c0008t0005g0179 |
2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.130+26219C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729697 | |||||||
chr4:140729818 | C | CA | 21 | a0001c0001t0001g0123 a0001c0001t0001g0164 a0001c0001t0001g0166 others(18): Show |
21 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+26097dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729818 | C | CAA | 84 | a0001c0001t0001g0004 a0001c0001t0001g0028 a0001c0001t0001g0093 others(81): Show |
85 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.130+26096_130+2609 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729818 | C | CAAA | 109 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
109 | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.130+26095_130+2609 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729818 | C | CAAAA | 21 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0020 others(18): Show |
21 | HG00423.hp1 HG00423.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.130+26094_130+2609 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729818 | CA | C | 10 | a0001c0001t0001g0117 a0001c0001t0003g0277 a0001c0002t0001g0245 others(7): Show |
10 | HG00099.hp1 HG00639.hp1 HG02300.hp1 others(7): Show |
intron_variant | MODIFIER | c.130+26097delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729818 | CAAAAAAA others(4): Show |
C | 4 | a0001c0001t0014g0284 a0001c0003t0003g0285 a0001c0004t0001g0087 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+26087_130+2609 others(15): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729818 | CAAAAAAA others(6): Show |
C | 1 | a0001c0002t0002g0088 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.130+26085_130+2609 others(17): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729818 | |||||||
chr4:140729875 | G | T | 6 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+26041C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140729875 | |||||||
chr4:140730280 | G | T | 259 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(256): Show |
260 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(257): Show |
intron_variant | MODIFIER | c.130+25636C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730280 | |||||||
chr4:140730438 | C | T | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.130+25478G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730438 | |||||||
chr4:140730572 | C | T | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+25344G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730572 | |||||||
chr4:140730664 | T | C | 1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+25252A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730664 | |||||||
chr4:140730703 | G | T | 13 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0249 others(10): Show |
13 | HG01346.hp2 HG01975.hp2 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.130+25213C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730703 | |||||||
chr4:140730722 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.130+25194A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730722 | |||||||
chr4:140730727 | A | G | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+25189T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730727 | |||||||
chr4:140730944 | G | A | 1 | a0001c0002t0001g0235 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.130+24972C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140730944 | |||||||
chr4:140731026 | T | A | 2 | a0001c0002t0002g0226 a0001c0002t0002g0232 |
2 | HG01346.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.130+24890A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731026 | |||||||
chr4:140731150 | T | C | 1 | a0001c0005t0001g0115 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.130+24766A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731150 | |||||||
chr4:140731206 | C | T | 4 | a0001c0004t0005g0266 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24710G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731206 | |||||||
chr4:140731214 | T | C | 2 | a0001c0005t0001g0146 a0001c0005t0001g0158 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.130+24702A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731214 | |||||||
chr4:140731360 | T | C | 2 | a0001c0001t0001g0004 a0001c0001t0001g0164 |
2 | HG01192.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.130+24556A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731360 | |||||||
chr4:140731376 | T | C | 4 | a0001c0004t0005g0266 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24540A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731376 | |||||||
chr4:140731503 | C | A | 1 | a0001c0001t0001g0064 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.130+24413G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731503 | |||||||
chr4:140731605 | T | C | 4 | a0001c0001t0014g0284 a0001c0003t0003g0285 a0001c0004t0001g0087 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24311A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731605 | |||||||
chr4:140731668 | T | C | 4 | a0001c0004t0005g0266 a0001c0008t0001g0241 a0001c0008t0005g0242 others(1): Show |
4 | HG01261.hp2 HG02886.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+24248A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731668 | |||||||
chr4:140731668 | T | TAC | 95 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0010 others(92): Show |
95 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(92): Show |
intron_variant | MODIFIER | c.130+24246_130+2424 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731668 | |||||||
chr4:140731693 | A | C | 26 | a0001c0001t0001g0144 a0001c0001t0001g0161 a0001c0001t0001g0162 others(23): Show |
26 | HG01070.hp2 HG01071.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.130+24223T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731693 | |||||||
chr4:140731694 | C | CAT | 18 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(15): Show |
18 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(15): Show |
intron_variant | MODIFIER | c.130+24221_130+2422 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731694 | |||||||
chr4:140731757 | G | C | 2 | a0001c0020t0001g0188 a0001c0021t0001g0265 |
2 | HG06807.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.130+24159C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731757 | |||||||
chr4:140731768 | A | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(131): Show |
135 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(132): Show |
intron_variant | MODIFIER | c.130+24148T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731768 | |||||||
chr4:140731852 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130+24064A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731852 | |||||||
chr4:140731899 | T | C | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.130+24017A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731899 | |||||||
chr4:140731901 | T | C | 1 | a0001c0002t0001g0245 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.130+24015A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140731901 | |||||||
chr4:140732078 | G | A | 5 | a0001c0001t0014g0284 a0001c0003t0003g0285 a0001c0004t0001g0087 others(2): Show |
5 | HG02615.hp2 HG02723.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+23838C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732078 | |||||||
chr4:140732114 | T | C | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+23802A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732114 | |||||||
chr4:140732166 | G | T | 8 | a0001c0003t0001g0097 a0001c0005t0001g0129 a0001c0005t0001g0130 others(5): Show |
8 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+23750C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732166 | |||||||
chr4:140732185 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+23731C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732185 | |||||||
chr4:140732243 | A | G | 6 | a0001c0004t0001g0047 a0002c0009t0002g0037 a0002c0009t0002g0040 others(3): Show |
6 | NA18966.hp1 NA18982.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+23673T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732243 | |||||||
chr4:140732377 | T | C | 1 | a0001c0016t0012g0272 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.130+23539A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732377 | |||||||
chr4:140732414 | C | A | 1 | a0001c0002t0001g0200 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.130+23502G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140732414 | |||||||
chr4:140733155 | C | G | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+22761G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733155 | |||||||
chr4:140733297 | A | AT | 8 | a0001c0003t0001g0097 a0001c0005t0001g0129 a0001c0005t0001g0130 others(5): Show |
8 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(5): Show |
intron_variant | MODIFIER | c.130+22618dupA | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733297 | |||||||
chr4:140733418 | T | A | 1 | a0001c0002t0001g0227 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.130+22498A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733418 | |||||||
chr4:140733484 | T | C | 9 | a0001c0001t0001g0185 a0001c0001t0001g0199 a0001c0002t0001g0189 others(6): Show |
9 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+22432A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733484 | |||||||
chr4:140733687 | G | A | 1 | a0001c0001t0004g0292 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.130+22229C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733687 | |||||||
chr4:140733754 | C | A | 1 | a0001c0006t0007g0228 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.130+22162G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140733754 | |||||||
chr4:140734022 | A | G | 80 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0185 others(77): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(78): Show |
intron_variant | MODIFIER | c.130+21894T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734022 | |||||||
chr4:140734292 | C | T | 2 | a0001c0004t0001g0229 a0001c0004t0002g0261 |
2 | HG03486.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.130+21624G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734292 | |||||||
chr4:140734326 | C | T | 131 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(128): Show |
132 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(129): Show |
intron_variant | MODIFIER | c.130+21590G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734326 | |||||||
chr4:140734327 | G | A | 7 | a0001c0001t0001g0135 a0001c0001t0002g0274 a0001c0002t0002g0088 others(4): Show |
7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+21589C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734327 | |||||||
chr4:140734377 | A | G | 7 | a0001c0001t0001g0135 a0001c0001t0002g0274 a0001c0002t0002g0088 others(4): Show |
7 | HG00639.hp2 HG02630.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.130+21539T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734377 | |||||||
chr4:140734520 | G | A | 83 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(80): Show |
83 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.130+21396C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734520 | |||||||
chr4:140734565 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0004t0005g0266 others(2): Show |
5 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+21351C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734565 | |||||||
chr4:140734636 | A | T | 1 | a0001c0001t0001g0251 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.130+21280T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734636 | |||||||
chr4:140734638 | T | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+21278A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734638 | |||||||
chr4:140734827 | A | G | 1 | a0001c0004t0001g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.130+21089T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140734827 | |||||||
chr4:140735191 | T | C | 104 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0144 others(101): Show |
105 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(102): Show |
intron_variant | MODIFIER | c.130+20725A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735191 | |||||||
chr4:140735256 | A | G | 1 | a0001c0001t0002g0244 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.130+20660T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735256 | |||||||
chr4:140735313 | G | A | 121 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(118): Show |
121 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(118): Show |
intron_variant | MODIFIER | c.130+20603C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735313 | |||||||
chr4:140735436 | G | A | 1 | a0001c0010t0001g0260 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.130+20480C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735436 | |||||||
chr4:140735449 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+20467G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735449 | |||||||
chr4:140735619 | G | A | 1 | a0001c0013t0011g0116 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.130+20297C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735619 | |||||||
chr4:140735683 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0011 |
2 | NA18972.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.130+20233G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735683 | |||||||
chr4:140735907 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+20009G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735907 | |||||||
chr4:140735930 | T | C | 2 | a0001c0002t0002g0088 a0001c0004t0001g0087 |
2 | HG00639.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.130+19986A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140735930 | |||||||
chr4:140736065 | C | T | 1 | a0001c0008t0001g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.130+19851G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736065 | |||||||
chr4:140736163 | G | GGGAGAGA others(11): Show |
3 | a0001c0001t0001g0010 a0001c0001t0001g0192 a0001c0003t0001g0086 |
3 | HG00544.hp2 NA18982.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.130+19735_130+1975 others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736163 | |||||||
chr4:140736350 | G | A | 6 | a0001c0001t0001g0161 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG01106.hp2 HG02055.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+19566C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736350 | |||||||
chr4:140736366 | C | T | 1 | a0001c0001t0001g0082 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.130+19550G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736366 | |||||||
chr4:140736465 | C | T | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.130+19451G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736465 | |||||||
chr4:140736499 | C | T | 1 | a0001c0001t0001g0249 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.130+19417G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736499 | |||||||
chr4:140736933 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+18983A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140736933 | |||||||
chr4:140737070 | A | C | 1 | a0001c0004t0005g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+18846T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737070 | |||||||
chr4:140737121 | G | A | 130 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0091 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.130+18795C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737121 | |||||||
chr4:140737436 | TTC | T | 9 | a0001c0001t0001g0024 a0001c0002t0001g0245 a0001c0002t0001g0268 others(6): Show |
9 | HG01167.hp2 HG01261.hp2 HG01943.hp1 others(6): Show |
intron_variant | MODIFIER | c.130+18478_130+1847 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | |||||||
chr4:140737436 | TTCTC | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0006 a0001c0001t0001g0007 others(100): Show |
103 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.130+18476_130+1847 others(8): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | |||||||
chr4:140737436 | TTCTCTC | T | 125 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(122): Show |
126 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.130+18474_130+1847 others(10): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | |||||||
chr4:140737436 | TTCTCTCT others(1): Show |
T | 9 | a0001c0002t0001g0100 a0001c0003t0001g0097 a0001c0005t0001g0129 others(6): Show |
9 | HG00099.hp1 HG00639.hp1 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+18472_130+1847 others(12): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | |||||||
chr4:140737436 | TTCTCTCT others(3): Show |
T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0154 a0001c0002t0001g0231 others(1): Show |
4 | HG01891.hp1 NA18953.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+18470_130+1847 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737436 | |||||||
chr4:140737465 | T | A | 19 | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0135 others(16): Show |
19 | HG00639.hp2 HG00642.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+18451A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737465 | |||||||
chr4:140737543 | T | C | 101 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.130+18373A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737543 | |||||||
chr4:140737723 | C | A | 2 | a0001c0008t0001g0241 a0001c0008t0005g0242 |
2 | HG01261.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130+18193G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140737723 | |||||||
chr4:140738154 | C | T | 1 | a0001c0002t0001g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+17762G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738154 | |||||||
chr4:140738336 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+17580G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738336 | |||||||
chr4:140738435 | T | C | 260 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(257): Show |
261 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(258): Show |
intron_variant | MODIFIER | c.130+17481A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738435 | |||||||
chr4:140738485 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+17431G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738485 | |||||||
chr4:140738699 | C | T | 5 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0004t0005g0266 others(2): Show |
5 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+17217G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738699 | |||||||
chr4:140738875 | T | A | 3 | a0001c0002t0001g0245 a0001c0002t0001g0268 a0001c0002t0001g0269 |
3 | HG02896.hp1 HG02897.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.130+17041A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738875 | |||||||
chr4:140738952 | G | A | 6 | a0001c0004t0001g0047 a0002c0009t0002g0037 a0002c0009t0002g0040 others(3): Show |
6 | NA18966.hp1 NA18982.hp1 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+16964C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140738952 | |||||||
chr4:140739047 | TTGCTGCC others(95): Show |
T | 1 | a0001c0005t0001g0172 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.130+16767_130+1686 others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739047 | |||||||
chr4:140739074 | G | A | 2 | a0001c0002t0001g0196 a0001c0002t0001g0246 |
2 | HG01243.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.130+16842C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739074 | |||||||
chr4:140739118 | T | A | 1 | a0001c0001t0001g0150 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.130+16798A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739118 | |||||||
chr4:140739141 | C | T | 6 | a0001c0001t0001g0204 a0001c0001t0001g0249 a0001c0002t0001g0190 others(3): Show |
6 | NA18941.hp2 NA18943.hp1 NA18944.hp2 others(3): Show |
intron_variant | MODIFIER | c.130+16775G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739141 | |||||||
chr4:140739173 | T | C | 130 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0091 others(127): Show |
131 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(128): Show |
intron_variant | MODIFIER | c.130+16743A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739173 | |||||||
chr4:140739192 | A | G | 1 | a0001c0003t0001g0072 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.130+16724T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739192 | |||||||
chr4:140739273 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+16643G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739273 | |||||||
chr4:140739277 | C | T | 17 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(14): Show |
17 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+16639G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739277 | |||||||
chr4:140739425 | C | A | 4 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(1): Show |
4 | HG01517.hp1 HG03704.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+16491G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739425 | |||||||
chr4:140739466 | G | T | 2 | a0001c0001t0001g0028 a0001c0001t0001g0029 |
2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.130+16450C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739466 | |||||||
chr4:140739834 | T | C | 89 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(86): Show |
89 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.130+16082A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739834 | |||||||
chr4:140739848 | A | T | 2 | a0001c0005t0002g0103 a0001c0005t0002g0104 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.130+16068T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739848 | |||||||
chr4:140739884 | A | G | 1 | a0001c0002t0001g0201 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.130+16032T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739884 | |||||||
chr4:140739971 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+15945A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140739971 | |||||||
chr4:140740195 | T | C | 17 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(14): Show |
17 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+15721A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740195 | |||||||
chr4:140740533 | A | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+15383T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740533 | |||||||
chr4:140740585 | G | A | 5 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0004t0005g0266 others(2): Show |
5 | HG01192.hp1 HG01261.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+15331C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740585 | |||||||
chr4:140740833 | G | A | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+15083C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740833 | |||||||
chr4:140740920 | T | C | 1 | a0001c0001t0001g0021 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.130+14996A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140740920 | |||||||
chr4:140741009 | T | C | 106 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0144 others(103): Show |
107 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(104): Show |
intron_variant | MODIFIER | c.130+14907A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741009 | |||||||
chr4:140741124 | C | T | 17 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(14): Show |
17 | HG01074.hp2 HG01081.hp1 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.130+14792G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741124 | |||||||
chr4:140741155 | A | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+14761T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741155 | |||||||
chr4:140741362 | A | G | 135 | a0001c0001t0001g0003 a0001c0001t0001g0028 a0001c0001t0001g0029 others(132): Show |
136 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.130+14554T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741362 | |||||||
chr4:140741442 | T | C | 3 | a0001c0001t0001g0024 a0001c0003t0001g0022 a0001c0003t0001g0023 |
3 | HG01167.hp2 HG01943.hp1 HG01978.hp2 |
intron_variant | MODIFIER | c.130+14474A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741442 | |||||||
chr4:140741524 | C | T | 2 | a0001c0002t0001g0095 a0001c0010t0001g0191 |
2 | NA19056.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.130+14392G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741524 | |||||||
chr4:140741932 | G | A | 2 | a0001c0001t0001g0026 a0001c0003t0001g0025 |
2 | NA18970.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.130+13984C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741932 | |||||||
chr4:140741991 | G | T | 9 | a0001c0001t0001g0185 a0001c0001t0001g0199 a0001c0002t0001g0189 others(6): Show |
9 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.130+13925C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140741991 | |||||||
chr4:140742179 | A | G | 1 | a0001c0002t0001g0098 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.130+13737T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742179 | |||||||
chr4:140742247 | T | C | 4 | a0001c0001t0014g0284 a0001c0003t0003g0285 a0001c0004t0001g0087 others(1): Show |
4 | HG02615.hp2 HG02723.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.130+13669A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742247 | |||||||
chr4:140742255 | C | T | 19 | a0001c0001t0001g0045 a0001c0001t0001g0077 a0001c0001t0001g0080 others(16): Show |
19 | HG00423.hp2 HG00609.hp1 HG00621.hp1 others(16): Show |
intron_variant | MODIFIER | c.130+13661G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742255 | |||||||
chr4:140742323 | G | A | 1 | a0001c0002t0001g0233 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.130+13593C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742323 | |||||||
chr4:140742442 | T | A | 4 | a0001c0001t0001g0073 a0001c0003t0001g0072 a0001c0003t0001g0074 others(1): Show |
4 | HG00408.hp1 HG00673.hp2 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+13474A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742442 | |||||||
chr4:140742531 | C | CA | 15 | a0001c0001t0001g0117 a0001c0001t0001g0135 a0001c0001t0002g0274 others(12): Show |
15 | HG00639.hp2 HG02056.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.130+13384dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | |||||||
chr4:140742531 | CA | C | 101 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(98): Show |
101 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.130+13384delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | |||||||
chr4:140742531 | CAA | C | 18 | a0001c0001t0001g0010 a0001c0001t0001g0139 a0001c0001t0001g0140 others(15): Show |
18 | HG01106.hp2 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.130+13383_130+1338 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | |||||||
chr4:140742531 | CAAA | C | 93 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0144 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+13382_130+1338 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742531 | |||||||
chr4:140742635 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+13281A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742635 | |||||||
chr4:140742888 | CAGG | C | 74 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0185 others(71): Show |
75 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.130+13025_130+1302 others(7): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742888 | |||||||
chr4:140742902 | G | A | 4 | a0001c0001t0002g0090 a0001c0001t0002g0157 a0001c0005t0001g0146 others(1): Show |
4 | HG02886.hp2 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+13014C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742902 | |||||||
chr4:140742977 | G | A | 2 | a0001c0001t0001g0167 a0001c0001t0001g0168 |
2 | HG01106.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.130+12939C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140742977 | |||||||
chr4:140743038 | G | A | 257 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(254): Show |
258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.130+12878C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743038 | |||||||
chr4:140743365 | C | T | 1 | a0001c0001t0002g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.130+12551G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743365 | |||||||
chr4:140743574 | G | C | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+12342C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743574 | |||||||
chr4:140743583 | T | C | 2 | a0001c0001t0002g0274 a0001c0005t0001g0172 |
2 | HG02965.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.130+12333A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743583 | |||||||
chr4:140743682 | C | T | 1 | a0001c0003t0001g0038 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.130+12234G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743682 | |||||||
chr4:140743684 | G | T | 1 | a0001c0004t0001g0143 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.130+12232C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743684 | |||||||
chr4:140743707 | A | G | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+12209T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743707 | |||||||
chr4:140743743 | C | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+12173G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743743 | |||||||
chr4:140743914 | C | T | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+12002G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743914 | |||||||
chr4:140743935 | T | G | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+11981A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140743935 | |||||||
chr4:140744036 | G | C | 126 | a0001c0001t0001g0003 a0001c0001t0001g0057 a0001c0001t0001g0058 others(123): Show |
127 | HG00099.hp2 HG00140.hp2 HG00609.hp2 others(124): Show |
intron_variant | MODIFIER | c.130+11880C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744036 | |||||||
chr4:140744133 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.130+11783C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744133 | |||||||
chr4:140744175 | T | C | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+11741A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744175 | |||||||
chr4:140744286 | A | C | 3 | a0001c0008t0001g0180 a0001c0008t0005g0179 a0001c0018t0001g0175 |
3 | HG02280.hp2 HG02809.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.130+11630T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744286 | |||||||
chr4:140744305 | C | T | 2 | a0001c0001t0001g0062 a0001c0001t0002g0244 |
2 | HG00733.hp2 HG01175.hp2 |
intron_variant | MODIFIER | c.130+11611G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744305 | |||||||
chr4:140744333 | A | G | 1 | a0001c0001t0001g0062 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.130+11583T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744333 | |||||||
chr4:140744357 | A | G | 1 | a0001c0001t0001g0144 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.130+11559T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744357 | |||||||
chr4:140744423 | T | G | 5 | a0001c0002t0001g0098 a0001c0002t0001g0100 a0001c0002t0001g0101 others(2): Show |
5 | HG00735.hp1 HG01884.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+11493A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744423 | |||||||
chr4:140744504 | G | C | 83 | a0001c0001t0001g0034 a0001c0001t0001g0185 a0001c0001t0001g0192 others(80): Show |
84 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.130+11412C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744504 | |||||||
chr4:140744693 | G | A | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+11223C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744693 | |||||||
chr4:140744798 | G | A | 2 | a0001c0001t0001g0003 a0001c0004t0001g0087 |
2 | HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.130+11118C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744798 | |||||||
chr4:140744879 | T | TA | 10 | a0001c0001t0001g0161 a0001c0001t0001g0178 a0001c0001t0016g0295 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.130+11036dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744879 | TA | T | 112 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
112 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.130+11036delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744879 | TAA | T | 91 | a0001c0001t0001g0077 a0001c0001t0001g0144 a0001c0001t0001g0145 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.130+11035_130+1103 others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744879 | TAAAAAAA others(3): Show |
T | 1 | a0001c0001t0001g0036 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.130+11027_130+1103 others(14): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744879 | TAAAAAAA others(4): Show |
T | 1 | a0001c0002t0001g0193 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.130+11026_130+1103 others(15): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744879 | TAAAAAAA others(5): Show |
T | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+11025_130+1103 others(16): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744879 | TAAAAAAA others(7): Show |
T | 2 | a0001c0004t0005g0266 a0001c0013t0011g0116 |
2 | HG02886.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.130+11023_130+1103 others(18): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744879 | |||||||
chr4:140744925 | C | A | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+10991G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744925 | |||||||
chr4:140744926 | C | T | 1 | a0001c0008t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.130+10990G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744926 | |||||||
chr4:140744954 | T | G | 1 | a0001c0006t0001g0236 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.130+10962A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744954 | |||||||
chr4:140744967 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+10949A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140744967 | |||||||
chr4:140745018 | C | A | 3 | a0001c0001t0001g0135 a0001c0002t0002g0088 a0001c0014t0001g0089 |
3 | HG00639.hp2 HG01361.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.130+10898G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745018 | |||||||
chr4:140745096 | T | C | 1 | a0001c0003t0001g0031 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.130+10820A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745096 | |||||||
chr4:140745105 | A | T | 12 | a0001c0001t0001g0135 a0001c0001t0002g0274 a0001c0002t0002g0088 others(9): Show |
12 | HG00639.hp1 HG00639.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+10811T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745105 | |||||||
chr4:140745196 | T | C | 8 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0002t0001g0098 others(5): Show |
8 | HG00735.hp1 HG01192.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+10720A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745196 | |||||||
chr4:140745339 | T | C | 1 | a0001c0001t0001g0061 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.130+10577A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745339 | |||||||
chr4:140745498 | T | C | 1 | a0001c0003t0001g0097 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.130+10418A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745498 | |||||||
chr4:140745504 | C | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+10412G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745504 | |||||||
chr4:140745553 | T | C | 2 | a0001c0008t0001g0186 a0001c0008t0002g0187 |
2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.130+10363A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745553 | |||||||
chr4:140745594 | T | C | 1 | a0001c0001t0003g0286 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.130+10322A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745594 | |||||||
chr4:140745789 | T | C | 68 | a0001c0001t0001g0004 a0001c0001t0001g0091 a0001c0001t0001g0093 others(65): Show |
68 | HG00735.hp1 HG01070.hp2 HG01071.hp2 others(65): Show |
intron_variant | MODIFIER | c.130+10127A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745789 | |||||||
chr4:140745839 | C | T | 1 | a0001c0004t0005g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+10077G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745839 | |||||||
chr4:140745988 | G | A | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+9928C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140745988 | |||||||
chr4:140746109 | C | T | 258 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(255): Show |
259 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.130+9807G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746109 | |||||||
chr4:140746207 | G | A | 1 | a0001c0002t0001g0237 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.130+9709C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746207 | |||||||
chr4:140746420 | A | G | 1 | a0001c0003t0001g0009 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.130+9496T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746420 | |||||||
chr4:140746500 | G | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0076 |
2 | HG01175.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.130+9416C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746500 | |||||||
chr4:140746637 | C | T | 2 | a0001c0005t0002g0103 a0001c0005t0002g0104 |
2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.130+9279G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746637 | |||||||
chr4:140746725 | T | C | 3 | a0001c0001t0001g0007 a0001c0001t0001g0063 a0001c0001t0001g0064 |
3 | HG03491.hp2 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.130+9191A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746725 | |||||||
chr4:140746888 | C | T | 2 | a0001c0001t0002g0183 a0001c0004t0001g0143 |
2 | HG03041.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.130+9028G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746888 | |||||||
chr4:140746891 | G | A | 3 | a0001c0004t0005g0266 a0001c0008t0001g0241 a0001c0008t0005g0242 |
3 | HG01261.hp2 HG02896.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.130+9025C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746891 | |||||||
chr4:140746926 | G | T | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+8990C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140746926 | |||||||
chr4:140747017 | A | AAAAT | 14 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0267 others(11): Show |
14 | HG00639.hp1 HG00735.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.130+8895_130+8898d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747017 | |||||||
chr4:140747017 | A | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+8899T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747017 | |||||||
chr4:140747021 | T | A | 38 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0001g0113 others(35): Show |
38 | HG00099.hp1 HG00408.hp2 HG00558.hp2 others(35): Show |
intron_variant | MODIFIER | c.130+8895A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747021 | |||||||
chr4:140747042 | G | A | 1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+8874C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747042 | |||||||
chr4:140747164 | G | A | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.130+8752C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747164 | |||||||
chr4:140747349 | C | CA | 87 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0192 others(84): Show |
88 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.130+8566dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747349 | |||||||
chr4:140747393 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.130+8523G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747393 | |||||||
chr4:140747473 | A | G | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130+8443T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747473 | |||||||
chr4:140747501 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+8415C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747501 | |||||||
chr4:140747517 | A | G | 85 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0192 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.130+8399T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747517 | |||||||
chr4:140747590 | T | A | 1 | a0001c0001t0001g0238 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.130+8326A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747590 | |||||||
chr4:140747613 | G | A | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+8303C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747613 | |||||||
chr4:140747735 | T | TA | 8 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0170 others(5): Show |
8 | HG00408.hp2 NA18944.hp1 NA18973.hp1 others(5): Show |
intron_variant | MODIFIER | c.130+8180_130+8181i others(3): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747735 | |||||||
chr4:140747743 | C | G | 1 | a0001c0001t0001g0164 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.130+8173G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747743 | |||||||
chr4:140747749 | T | C | 2 | a0001c0002t0001g0181 a0001c0002t0001g0243 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.130+8167A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140747749 | |||||||
chr4:140748184 | A | C | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+7732T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748184 | |||||||
chr4:140748469 | G | A | 1 | a0001c0001t0001g0141 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.130+7447C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748469 | |||||||
chr4:140748533 | G | C | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+7383C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748533 | |||||||
chr4:140748653 | A | G | 1 | a0001c0004t0005g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+7263T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748653 | |||||||
chr4:140748654 | C | T | 2 | a0001c0002t0001g0095 a0001c0010t0001g0191 |
2 | NA19056.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.130+7262G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748654 | |||||||
chr4:140748730 | A | G | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.130+7186T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748730 | |||||||
chr4:140748942 | G | A | 2 | a0001c0001t0001g0006 a0001c0001t0001g0062 |
2 | HG00733.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.130+6974C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748942 | |||||||
chr4:140748989 | G | A | 1 | a0001c0001t0017g0297 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.130+6927C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140748989 | |||||||
chr4:140749073 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.130+6843A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749073 | |||||||
chr4:140749116 | A | G | 1 | a0001c0004t0005g0266 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.130+6800T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749116 | |||||||
chr4:140749253 | G | T | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+6663C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749253 | |||||||
chr4:140749272 | T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+6644A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749272 | |||||||
chr4:140749601 | T | C | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.130+6315A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749601 | |||||||
chr4:140749651 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.130+6265G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749651 | |||||||
chr4:140749674 | T | C | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+6242A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749674 | |||||||
chr4:140749717 | C | T | 36 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0034 others(33): Show |
36 | HG00140.hp1 HG00423.hp2 HG00609.hp1 others(33): Show |
intron_variant | MODIFIER | c.130+6199G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749717 | |||||||
chr4:140749745 | A | G | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 |
3 | HG01255.hp2 HG02004.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.130+6171T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749745 | |||||||
chr4:140749866 | T | C | 1 | a0001c0001t0002g0090 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.130+6050A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749866 | |||||||
chr4:140749980 | T | C | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+5936A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140749980 | |||||||
chr4:140750080 | G | A | 4 | a0001c0004t0001g0124 a0001c0004t0001g0126 a0001c0004t0002g0127 others(1): Show |
4 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.130+5836C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750080 | |||||||
chr4:140750119 | A | T | 1 | a0001c0001t0006g0142 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.130+5797T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750119 | |||||||
chr4:140750159 | T | A | 1 | a0001c0002t0001g0065 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.130+5757A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750159 | |||||||
chr4:140750159 | T | TA | 192 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(189): Show |
193 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.130+5756dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750159 | |||||||
chr4:140750172 | T | A | 3 | a0001c0001t0001g0093 a0001c0001t0001g0094 a0001c0002t0002g0092 |
3 | HG02615.hp1 HG02717.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.130+5744A>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750172 | |||||||
chr4:140750235 | G | T | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130+5681C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750235 | |||||||
chr4:140750419 | C | T | 1 | a0001c0001t0001g0066 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.130+5497G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750419 | |||||||
chr4:140750493 | A | G | 2 | a0001c0002t0001g0268 a0001c0002t0001g0269 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.130+5423T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750493 | |||||||
chr4:140750624 | G | A | 91 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0185 others(88): Show |
92 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(89): Show |
intron_variant | MODIFIER | c.130+5292C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750624 | |||||||
chr4:140750692 | C | T | 1 | a0001c0004t0001g0087 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.130+5224G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750692 | |||||||
chr4:140750795 | T | C | 30 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+5121A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750795 | |||||||
chr4:140750806 | TGCAAGCT others(13): Show |
T | 1 | a0001c0001t0001g0008 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.130+5090_130+5109d others(22): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750806 | |||||||
chr4:140750975 | T | TA | 12 | a0001c0001t0001g0135 a0001c0001t0002g0274 a0001c0002t0002g0088 others(9): Show |
12 | HG00639.hp1 HG00639.hp2 HG01361.hp2 others(9): Show |
intron_variant | MODIFIER | c.130+4940dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140750975 | |||||||
chr4:140751349 | A | G | 1 | a0001c0001t0001g0007 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.130+4567T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751349 | |||||||
chr4:140751494 | T | G | 256 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(253): Show |
257 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.130+4422A>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751494 | |||||||
chr4:140751533 | T | C | 1 | a0001c0001t0005g0096 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.130+4383A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751533 | |||||||
chr4:140751641 | C | T | 2 | a0001c0002t0001g0181 a0001c0002t0001g0243 |
2 | HG02145.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.130+4275G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751641 | |||||||
chr4:140751760 | T | C | 1 | a0001c0020t0001g0188 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.130+4156A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751760 | |||||||
chr4:140751775 | G | A | 5 | a0001c0002t0001g0138 a0001c0002t0001g0174 a0001c0004t0001g0136 others(2): Show |
5 | HG00741.hp1 HG01256.hp2 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.130+4141C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751775 | |||||||
chr4:140751947 | T | C | 1 | a0001c0014t0001g0089 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.130+3969A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140751947 | |||||||
chr4:140752057 | C | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0182 others(90): Show |
94 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.130+3859G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752057 | |||||||
chr4:140752129 | C | A | 1 | a0001c0004t0001g0273 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.130+3787G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752129 | |||||||
chr4:140752193 | G | T | 1 | a0001c0002t0001g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130+3723C>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752193 | |||||||
chr4:140752360 | TA | T | 92 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0182 others(89): Show |
93 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.130+3555delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752360 | |||||||
chr4:140752442 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.130+3474G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752442 | |||||||
chr4:140752566 | T | TA | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.130+3349dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752566 | |||||||
chr4:140752838 | C | G | 30 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(27): Show |
30 | HG01106.hp2 HG01884.hp2 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.130+3078G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752838 | |||||||
chr4:140752902 | A | G | 2 | a0001c0001t0002g0090 a0001c0003t0001g0097 |
2 | HG00099.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.130+3014T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752902 | |||||||
chr4:140752920 | G | A | 5 | a0001c0001t0001g0066 a0001c0001t0001g0082 a0001c0001t0001g0083 others(2): Show |
5 | HG00621.hp2 HG02056.hp2 NA18941.hp1 others(2): Show |
intron_variant | MODIFIER | c.130+2996C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140752920 | |||||||
chr4:140753037 | C | T | 1 | a0001c0002t0003g0275 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.130+2879G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753037 | |||||||
chr4:140753040 | A | T | 1 | a0001c0018t0001g0175 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.130+2876T>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753040 | |||||||
chr4:140753070 | G | C | 1 | a0001c0001t0004g0296 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.130+2846C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753070 | |||||||
chr4:140753086 | G | C | 1 | a0001c0021t0001g0265 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.130+2830C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753086 | |||||||
chr4:140753295 | T | C | 3 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0141 |
3 | HG02630.hp2 HG03540.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.130+2621A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753295 | |||||||
chr4:140753307 | C | T | 85 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0001g0192 others(82): Show |
86 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.130+2609G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753307 | |||||||
chr4:140753388 | C | G | 1 | a0001c0005t0009g0005 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.130+2528G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753388 | |||||||
chr4:140753447 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.130+2469C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753447 | |||||||
chr4:140753535 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+2381T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753535 | |||||||
chr4:140753675 | T | C | 1 | a0001c0003t0001g0240 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.130+2241A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753675 | |||||||
chr4:140753893 | G | A | 1 | a0001c0002t0001g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.130+2023C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140753893 | |||||||
chr4:140754046 | T | C | 59 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(56): Show |
59 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.130+1870A>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754046 | |||||||
chr4:140754388 | C | T | 59 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(56): Show |
59 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.130+1528G>A | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754388 | |||||||
chr4:140754545 | A | C | 1 | a0001c0002t0001g0189 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.130+1371T>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754545 | |||||||
chr4:140754604 | G | A | 59 | a0001c0001t0001g0091 a0001c0001t0001g0093 a0001c0001t0001g0094 others(56): Show |
59 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(56): Show |
intron_variant | MODIFIER | c.130+1312C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754604 | |||||||
chr4:140754614 | C | CA | 56 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0001c0001t0001g0073 others(53): Show |
56 | HG00408.hp1 HG00544.hp1 HG00621.hp2 others(53): Show |
intron_variant | MODIFIER | c.130+1301dupT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | |||||||
chr4:140754614 | C | CAA | 14 | a0001c0001t0001g0182 a0001c0001t0001g0185 a0001c0001t0002g0183 others(11): Show |
14 | HG01515.hp1 HG02451.hp2 HG02559.hp2 others(11): Show |
intron_variant | MODIFIER | c.130+1300_130+1301d others(4): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | |||||||
chr4:140754614 | C | CAAA | 55 | a0001c0001t0001g0192 a0001c0001t0001g0195 a0001c0001t0001g0199 others(52): Show |
56 | HG00099.hp2 HG00140.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.130+1299_130+1301d others(5): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | |||||||
chr4:140754614 | C | CAAAA | 24 | a0001c0001t0001g0249 a0001c0001t0001g0251 a0001c0001t0001g0257 others(21): Show |
24 | HG01167.hp1 HG01175.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.130+1298_130+1301d others(6): Show |
TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | |||||||
chr4:140754614 | CA | C | 11 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0093 others(8): Show |
11 | HG00639.hp2 HG01361.hp2 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.130+1301delT | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754614 | |||||||
chr4:140754804 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.130+1112C>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754804 | |||||||
chr4:140754936 | C | A | 6 | a0001c0001t0001g0271 a0001c0001t0002g0270 a0001c0002t0001g0268 others(3): Show |
6 | HG02486.hp1 HG02559.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.130+980G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140754936 | |||||||
chr4:140755501 | C | A | 1 | a0001c0003t0001g0086 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.130+415G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755501 | |||||||
chr4:140755507 | C | A | 22 | a0001c0001t0003g0277 a0001c0001t0003g0278 a0001c0001t0003g0279 others(19): Show |
22 | HG01070.hp2 HG01071.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.130+409G>T | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755507 | |||||||
chr4:140755755 | A | G | 82 | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0008 others(79): Show |
82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.130+161T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755755 | |||||||
chr4:140755817 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.130+99T>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755817 | |||||||
chr4:140755838 | C | G | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.130+78G>C | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755838 | |||||||
chr4:140755901 | G | C | 1 | a0001c0001t0002g0274 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.130+15C>G | TBC1D9 | ENSG00000109436.8 | transcript | ENST00000442267.3 | protein_coding | 1/20 | chr4 | 140755901 |