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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr5
13823588
T
A
intron_variant
MODIFIER
DNAH5
c.6580-109A>T
chr5
13817881
G
A
intron_variant
MODIFIER
DNAH5
c.6842-78C>T
chr5
13810529
C
G
intron_variant
MODIFIER
DNAH5
c.7408-160G>C
chr5
13810451
CAT
C
intron_variant
MODIFIER
DNAH5
c.7408-84_7408-83delAT
chr5
13810441
G
A
intron_variant
MODIFIER
DNAH5
c.7408-72C>T
chr5
13810149
G
A
intron_variant
MODIFIER
DNAH5
c.7609+19C>T
chr5
13809957
G
T
intron_variant
MODIFIER
DNAH5
c.7609+211C>A
chr5
13788886
C
A
missense_variant
MODERATE
DNAH5
c.8586G>T
chr5
13776487
C
T
intron_variant
MODIFIER
DNAH5
c.9373+61G>A
chr5
13770757
C
CA
intron_variant
MODIFIER
DNAH5
c.9605+100_9605+101insT
chr5
13769257
T
A
intron_variant
MODIFIER
DNAH5
c.9721-12A>T
chr5
13719089
G
A
missense_variant
MODERATE
DNAH5
c.12401C>T
chr5
13719022
T
G
synonymous_variant
LOW
DNAH5
c.12468A>C
chr5
13714740
G
A
intron_variant
MODIFIER
DNAH5
c.12910-11C>T
chr5
13701654
T
C
intron_variant
MODIFIER
DNAH5
c.13339-109A>G
chr5
13701617
GA
G
intron_variant
MODIFIER
DNAH5
c.13339-73delT
chr5
13701536
T
C
missense_variant
MODERATE
DNAH5
c.13348A>G
chr5
13701525
T
C
synonymous_variant
LOW
DNAH5
c.13359A>G
chr5
13701327
A
G
intron_variant
MODIFIER
DNAH5
c.13491+66T>C
chr5
13692279
A
T
intron_variant
MODIFIER
DNAH5
c.13724-35T>A