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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr1
218610662
CT
C
intron_variant
MODIFIER
TGFB2
c.1017-22delT
chr1
204518842
C
A
3_prime_UTR_variant
MODIFIER
MDM4
c.*32C>A
chr1
204516025
A
G
intron_variant
MODIFIER
MDM4
c.903+20A>G
chr1
204515863
C
T
intron_variant
MODIFIER
MDM4
c.823-62C>T
chr1
204512100
T
C
intron_variant
MODIFIER
MDM4
c.672+28T>C
chr1
204506107
C
T
intron_variant
MODIFIER
MDM4
c.344-451C>T
chr1
204501383
C
T
intron_variant
MODIFIER
MDM4
c.343+9C>T
chr1
204495595
G
GT
intron_variant
MODIFIER
MDM4
c.153+33_153+34insT
chr1
201341341
C
T
intron_variant
MODIFIER
TNNT2
c.42-58G>A
chr1
201341175
CAGAAG
C
splice_region_variant&intron_variant
LOW
TNNT2
c.53-11_53-7delCTTCT
chr1
201339043
C
T
intron_variant
MODIFIER
TNNT2
c.68-70G>A
chr1
201338896
T
C
intron_variant
MODIFIER
TNNT2
c.97+48A>G
chr1
201338586
A
G
intron_variant
MODIFIER
TNNT2
c.97+358T>C
chr1
201338553
T
C
intron_variant
MODIFIER
TNNT2
c.97+391A>G
chr1
201337170
A
G
intron_variant
MODIFIER
TNNT2
c.163+120T>C
chr1
201335899
C
T
intron_variant
MODIFIER
TNNT2
c.233+67G>A
chr1
201334382
G
A
synonymous_variant
LOW
TNNT2
c.348C>T
chr1
201331664
C
A
intron_variant
MODIFIER
TNNT2
c.601-421G>T
chr1
201331554
T
G
intron_variant
MODIFIER
TNNT2
c.601-311A>C
chr1
155880760
C
CA
intron_variant
MODIFIER
RIT1
c.-3+273_-3+274insT