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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
179615887
T
C
missense_variant
MODERATE
TTN
c.11240A>G
chr2
179614952
A
G
synonymous_variant
LOW
TTN
c.12175T>C
chr2
179605180
C
T
synonymous_variant
LOW
TTN
c.12780G>A
chr2
179600563
G
A
synonymous_variant
LOW
TTN
c.14610C>T
chr2
179597259
T
C
missense_variant
MODERATE
TTN
c.16529A>G
chr2
179595117
C
G
intron_variant
MODIFIER
TTN
c.18029-19G>C
chr2
179587687
T
C
intron_variant
MODIFIER
TTN
c.21962-23A>G
chr2
179587130
C
G
missense_variant
MODERATE
TTN
c.22384G>C
chr2
179585393
A
G
splice_region_variant&intron_variant
LOW
TTN
c.23099-3T>C
chr2
179585266
C
T
synonymous_variant
LOW
TTN
c.23223G>A
chr2
179583496
T
G
missense_variant
MODERATE
TTN
c.24431A>C
chr2
179583398
T
C
intron_variant
MODIFIER
TTN
c.24505+24A>G
chr2
179582605
A
G
intron_variant
MODIFIER
TTN
c.25063+65T>C
chr2
179582537
G
T
missense_variant&splice_region_variant
MODERATE
TTN
c.25064C>A
chr2
179582327
C
T
missense_variant
MODERATE
TTN
c.25274G>A
chr2
179582162
C
T
intron_variant
MODIFIER
TTN
c.25352-53G>A
chr2
179580583
T
C
intron_variant
MODIFIER
TTN
c.25640-82A>G
chr2
179580093
A
C
intron_variant
MODIFIER
TTN
c.25922-102T>G
chr2
179579822
T
A
synonymous_variant
LOW
TTN
c.26091A>T
chr2
179579212
T
C
synonymous_variant
LOW
TTN
c.26289A>G