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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr5
13876664
T
C
intron_variant
MODIFIER
DNAH5
c.3396+129A>G
chr5
13871925
A
G
intron_variant
MODIFIER
DNAH5
c.3397-51T>C
chr5
13868103
TA
T
splice_region_variant&intron_variant
LOW
DNAH5
c.3835-3delT
chr5
13867819
C
T
intron_variant
MODIFIER
DNAH5
c.4053+64G>A
chr5
13866450
A
G
intron_variant
MODIFIER
DNAH5
c.4054-59T>C
chr5
13865980
T
C
synonymous_variant
LOW
DNAH5
c.4152A>G
chr5
13865717
A
G
intron_variant
MODIFIER
DNAH5
c.4355+60T>C
chr5
13864728
C
A
synonymous_variant
LOW
DNAH5
c.4374G>T
chr5
13862616
C
T
intron_variant
MODIFIER
DNAH5
c.4796+41G>A
chr5
13859743
G
T
intron_variant
MODIFIER
DNAH5
c.4797-29C>A
chr5
13851016
C
T
intron_variant
MODIFIER
DNAH5
c.4951-92G>A
chr5
13850750
A
G
intron_variant
MODIFIER
DNAH5
c.5114+11T>C
chr5
13850739
T
A
intron_variant
MODIFIER
DNAH5
c.5114+22A>T
chr5
13845151
C
G
intron_variant
MODIFIER
DNAH5
c.5115-49G>C
chr5
13845107
A
G
splice_region_variant&intron_variant
LOW
DNAH5
c.5115-5T>C
chr5
13845045
G
A
synonymous_variant
LOW
DNAH5
c.5172C>T
chr5
13839695
C
T
intron_variant
MODIFIER
DNAH5
c.5710-58G>A
chr5
13830048
G
A
intron_variant
MODIFIER
DNAH5
c.6249+87C>T
chr5
13829799
G
A
synonymous_variant
LOW
DNAH5
c.6264C>T
chr5
13829608
G
A
intron_variant
MODIFIER
DNAH5
c.6444+11C>T