|
|
| ID |
404 |
| OMIM_ID |
114480
|
| Disease |
BREAST CANCER |
| Gene |
BRCA1
|
| SNP_ID |
rs5821342
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/A
|
| Orientation |
fwd/B |
| Chr-Number |
17 |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
ttcggcatccaatggaagtctccgaaaaaa |
| 3'
Near Seq 30 bp |
aaaaaaaaaaacaagggctcaaggtacgcg |
| Fasta
Sequence |
GTGGACTTCC CTCCGACTTG CCTGTCTGGA GGGAAACCGA AGCAACGCTC TGAGCTCCGA
TTCACTGAAG AAAAGGAAAG GAAACCGACT TCTGAGAGCA AATAAAGCGG AGCCCTGGAA
GAGAAGAAAG GGCACGAGCC CTTCCTCCTC CCTCTTCCTG GGGGTGCTGC TACTTCCCCG
GCCTTGTGTG CAGGACTGGG GCCGCCGTTA CCTTTCCTCG ACCCACCAGA CCCCTCAACC
ACACAACCCG AGACGAATTC CCGCCTCCCG CCCCCTCGAC TCCCAGCGCC CAATAGCCCA
GCGAGCTCGA CCAATCACCC GCCAAGGCCA GGAATCAACC AGTCCCGGTG CGAGGTGAGG
GGGCGAGAAC TTCGGCATCC AATGGAAGTC TCCGAAAAAA
N
AAAAAAAAAA ACAAGGGCTC AAGGTACGCG GCGGAAGGTT GTCGCCACTC CAGCAAATCC
CTAGTGTTTG TTTAAAGTAG AAAGTCGTCT CAGTTTGACT TTTGAAACCG GCGATAGAGT
CTATGCAGCA AATTCCTTGG AAACTGGAAG TCTCATTCTT CACGTCCGTA GACCAGCGGA
AAGGAAGTAT CTTTAAGCTT TGCCAAGTTC TTTGAGCATT TATCAGTGCC ACTCAATTTA
AATTACCCAG CTTTGCAGTA GCCAGGATAG CGAAGACTCA GGCGGGAATT GCCAGACTGC
TGAGCCAAAC TTAAGTAAGA AGGCTCTGTG ACATCGGGCT ACAATCTATC TTTCATAATA
TTCAAGGCTT TCCCGGATGC TAAAATAAGC CAGAGACAAG
|
|
|
