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CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr15
67003841
C
T
intron_variant
MODIFIER
SMAD6
c.818-165C>T
chr15
66773975
G
A
intron_variant
MODIFIER
MAP2K1
c.569-118G>A
chr15
66745890
G
A
intron_variant
MODIFIER
MAP2K1
c.568+8845G>A
chr15
66737133
C
T
intron_variant
MODIFIER
MAP2K1
c.568+88C>T
chr15
66735551
C
T
intron_variant
MODIFIER
MAP2K1
c.439-67C>T
chr15
66679649
T
TC
5_prime_UTR_variant
MODIFIER
MAP2K1
c.-31dupC
chr15
66679601
G
C
5_prime_UTR_variant
MODIFIER
MAP2K1
c.-85G>C
chr15
63363401
C
CATTTTGTTTT
3_prime_UTR_variant
MODIFIER
TPM1
c.*30_*31insATTTTGTTTT
chr15
63353760
C
A
intron_variant
MODIFIER
TPM1
c.639+288C>A
chr15
63351840
C
A
synonymous_variant
LOW
TPM1
c.453C>A
chr15
63351687
A
G
intron_variant
MODIFIER
TPM1
c.375-75A>G
chr15
63349096
G
A
intron_variant
MODIFIER
TPM1
c.241-88G>A
chr15
63340990
C
T
intron_variant
MODIFIER
TPM1
c.240+4639C>T
chr15
63340989
C
CG
intron_variant
MODIFIER
TPM1
c.240+4638_240+4639insG
chr15
63340705
C
T
5_prime_UTR_variant
MODIFIER
TPM1
c.-70C>T
chr15
63340647
A
G
5_prime_UTR_variant
MODIFIER
TPM1
c.-128A>G
chr15
63340607
T
C
intron_variant
MODIFIER
TPM1
c.240+4256T>C
chr15
63334823
G
A
upstream_gene_variant
MODIFIER
TPM1
c.-192G>A
chr15
49097734
T
C
intron_variant
MODIFIER
CEP152
c.87+26A>G
chr15
49097645
T
A
intron_variant
MODIFIER
CEP152
c.87+115A>T