Page size
CHROM
POS
REF
ALT
Gene
HGVS.c
HGVS.p
dbSNP142 ID
chr3
10089841
C
A
intron_variant
MODIFIER
FANCD2
c.1413+106C>A
chr3
10089834
A
T
intron_variant
MODIFIER
FANCD2
c.1413+99A>T
chr3
10089828
G
A
intron_variant
MODIFIER
FANCD2
c.1413+93G>A
chr3
10089818
C
T
intron_variant
MODIFIER
FANCD2
c.1413+83C>T
chr3
10089815
A
C
intron_variant
MODIFIER
FANCD2
c.1413+80A>C
chr3
10089775
A
G
intron_variant
MODIFIER
FANCD2
c.1413+40A>G
chr3
10089772
C
G
intron_variant
MODIFIER
FANCD2
c.1413+37C>G
chr3
10089749
T
C
intron_variant
MODIFIER
FANCD2
c.1413+14T>C
chr3
10089738
A
G
splice_region_variant&intron_variant
LOW
FANCD2
c.1413+3A>G
chr3
10089723
G
A
synonymous_variant
LOW
FANCD2
c.1401G>A
chr3
10088461
T
C
intron_variant
MODIFIER
FANCD2
c.1278+54T>C
chr3
10088444
A
G
intron_variant
MODIFIER
FANCD2
c.1278+37A>G
chr3
10088443
C
A
intron_variant
MODIFIER
FANCD2
c.1278+36C>A
chr3
10088422
C
T
intron_variant
MODIFIER
FANCD2
c.1278+15C>T
chr3
10088409
TAAG
T
splice_region_variant&intron_variant
LOW
FANCD2
c.1278+3_1278+5delAAG
chr3
10088407
AG
A
splice_donor_variant&intron_variant
HIGH
FANCD2
c.1278+1delG
chr3
10088404
C
T
synonymous_variant
LOW
FANCD2
c.1275C>T
chr3
10088343
A
G
missense_variant
MODERATE
FANCD2
c.1214A>G
chr3
10088308
T
C
synonymous_variant
LOW
FANCD2
c.1179T>C
chr3
10088299
C
T
synonymous_variant
LOW
FANCD2
c.1170C>T