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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr2
179592735
C
A
intron_variant
MODIFIER
TTN
c.19714+102G>T
chr2
179592724
A
G
intron_variant
MODIFIER
TTN
c.19714+113T>C
chr2
179592161
A
G
intron_variant
MODIFIER
TTN
c.19994-63T>C
chr2
179587687
T
C
intron_variant
MODIFIER
TTN
c.21962-23A>G
chr2
179585963
A
G
intron_variant
MODIFIER
TTN
c.22817-34T>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
179582537
G
T
missense_variant&splice_region_variant
MODERATE
TTN
c.25064C>A
chr2
179581835
C
A
missense_variant
MODERATE
TTN
c.25626G>T
chr2
179580583
T
C
intron_variant
MODIFIER
TTN
c.25640-82A>G
chr2
179580434
A
G
synonymous_variant
LOW
TTN
c.25707T>C
chr2
179580068
A
C
intron_variant
MODIFIER
TTN
c.25922-77T>G
chr2
179579822
T
A
synonymous_variant
LOW
TTN
c.26091A>T
chr2
179579694
T
A
intron_variant
MODIFIER
TTN
c.26200+19A>T
chr2
179579366
G
A
intron_variant
MODIFIER
TTN
c.26201-66C>T
chr2
179579212
T
C
synonymous_variant
LOW
TTN
c.26289A>G
chr2
179578937
A
G
intron_variant
MODIFIER
TTN
c.26483-35T>C
chr2
179578730
G
A
synonymous_variant
LOW
TTN
c.26655C>T
chr2
179578108
T
TACAAAACAAAACAAAACAAAACAAA
intron_variant
MODIFIER
TTN
c.26762-10_26762-9insTTTGTTTTGTTTTGTTTTGTTTTGT
chr2
179576596
A
T
intron_variant
MODIFIER
TTN
c.27886+75T>A