Page size
CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
179579093
T
C
missense_variant
MODERATE
TTN
c.26408A>G
chr2
179578730
G
A
synonymous_variant
LOW
TTN
c.26655C>T
chr2
179578108
T
TACAAA
intron_variant
MODIFIER
TTN
c.26762-10_26762-9insTTTGT
chr2
179576596
A
T
intron_variant
MODIFIER
TTN
c.27886+75T>A
chr2
179571595
C
T
missense_variant
MODERATE
TTN
c.29128G>A
chr2
179569384
C
A
stop_gained
HIGH
TTN
c.29815G>T
chr2
179566146
T
G
intron_variant
MODIFIER
TTN
c.30598+109A>C
chr2
179558366
T
C
missense_variant
MODERATE
TTN
c.31564A>G
chr2
179558282
T
A
intron_variant
MODIFIER
TTN
c.31594+54A>T
chr2
179552906
A
G
missense_variant
MODERATE
TTN
c.32243T>C
chr2
179548954
T
TCAA
intron_variant
MODIFIER
TTN
c.32722+102_32722+103insTTG
chr2
179547860
A
G
intron_variant
MODIFIER
TTN
c.32887+78T>C
chr2
179543217
C
T
synonymous_variant
LOW
TTN
c.33834G>A
chr2
179541899
C
G
intron_variant
MODIFIER
TTN
c.34378+29G>C
chr2
179464527
T
C
missense_variant
MODERATE
TTN
c.56101A>G
chr2
179458591
C
T
missense_variant
MODERATE
TTN
c.58436G>A
chr2
179457147
G
A
missense_variant
MODERATE
TTN
c.59585C>T
chr2
179455207
T
C
synonymous_variant
LOW
TTN
c.61245A>G
chr2
179454394
A
G
synonymous_variant
LOW
TTN
c.62058T>C
chr2
179451420
G
A
missense_variant
MODERATE
TTN
c.64208C>T