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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr19
11327571
C
T
intron_variant
MODIFIER
DOCK6
c.3894+19G>A
chr19
11326629
C
A
intron_variant
MODIFIER
DOCK6
c.3895-26G>T
chr19
11326125
C
T
synonymous_variant
LOW
DOCK6
c.4044G>A
chr19
11326119
A
G
synonymous_variant
LOW
DOCK6
c.4050T>C
chr19
11325924
C
G
intron_variant
MODIFIER
DOCK6
c.4106+139G>C
chr19
11325417
A
G
intron_variant
MODIFIER
DOCK6
c.4107-92T>C
chr19
11324890
T
C
intron_variant
MODIFIER
DOCK6
c.4338+61A>G
chr19
11322980
T
C
intron_variant
MODIFIER
DOCK6
c.4492-153A>G
chr19
11319491
G
A
synonymous_variant
LOW
DOCK6
c.4959C>T
chr19
11314807
CTGGGGATGAGGAG
C
intron_variant
MODIFIER
DOCK6
c.5221-49_5221-37delCTCCTCATCCCCA
chr19
11313256
G
A
splice_region_variant&intron_variant
LOW
DOCK6
c.5361+4C>T
chr19
11310920
C
T
intron_variant
MODIFIER
DOCK6
c.6101+64G>A
chr19
11310290
TTCC
T
intron_variant
MODIFIER
DOCK6
c.6102-78_6102-76delGGA
chr19
11175851
A
G
downstream_gene_variant
MODIFIER
SMARCA4
c.*5114A>G
chr19
11172299
G
A
intron_variant
MODIFIER
SMARCA4
c.5008-161G>A
chr19
11170839
T
C
synonymous_variant
LOW
SMARCA4
c.4983T>C
chr19
11168896
A
G
intron_variant
MODIFIER
SMARCA4
c.4521-35A>G
chr19
11143811
C
G
intron_variant
MODIFIER
SMARCA4
c.3547-155C>G
chr19
11136315
C
T
intron_variant
MODIFIER
SMARCA4
c.3168+131C>T
chr19
11136215
C
G
intron_variant
MODIFIER
SMARCA4
c.3168+31C>G