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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
179574384
C
T
synonymous_variant
LOW
TTN
c.28662G>A
chr2
179570122
C
A
intron_variant
MODIFIER
TTN
c.29421-38G>T
chr2
179570114
A
T
intron_variant
MODIFIER
TTN
c.29421-30T>A
chr2
179569436
A
G
synonymous_variant
LOW
TTN
c.29763T>C
chr2
179569400
C
T
synonymous_variant
LOW
TTN
c.29799G>A
chr2
179566146
T
G
intron_variant
MODIFIER
TTN
c.30598+109A>C
chr2
179566091
C
CT
intron_variant
MODIFIER
TTN
c.30599-162_30599-161insA
chr2
179559943
A
C
intron_variant
MODIFIER
TTN
c.31270+132T>G
chr2
179558366
T
C
missense_variant
MODERATE
TTN
c.31564A>G
chr2
179558282
T
A
intron_variant
MODIFIER
TTN
c.31594+54A>T
chr2
179554305
C
T
missense_variant
MODERATE
TTN
c.31864G>A
chr2
179553917
G
A
intron_variant
MODIFIER
TTN
c.32012-54C>T
chr2
179541899
C
G
intron_variant
MODIFIER
TTN
c.34378+29G>C
chr2
179528378
C
T
missense_variant
MODERATE
TTN
c.36508G>A
chr2
179526573
A
G
splice_region_variant&intron_variant
LOW
TTN
c.37202-4T>C
chr2
179523514
T
A
missense_variant
MODERATE
TTN
c.37461A>T
chr2
179518052
A
G
splice_region_variant&intron_variant
LOW
TTN
c.38708-4T>C
chr2
179518003
A
G
missense_variant
MODERATE
TTN
c.38753T>C
chr2
179517654
T
C
synonymous_variant
LOW
TTN
c.38880A>G
chr2
179500790
A
G
synonymous_variant
LOW
TTN
c.41508T>C