|
|
| ID |
12 |
| OMIM_ID |
266300
|
| Disease |
SKIN/HAIR/EYE PIGMENTATION, VARIATION IN, 2; SHEP2 |
| Gene |
MC1R
|
| SNP_ID |
rs11310902
|
| Organism |
human (Homo sapiens) |
| Variation
Class |
DIP:
deletion/insertion polymorphism
|
| Alleles |
-/T
|
| Orientation |
fwd/T |
| Chr-Number |
16 |
| SNP
type |
N |
| Length |
801 |
| 5'
Near Seq 30 bp |
actgtgcccggcaataataatttttttttt |
| 3'
Near Seq 30 bp |
tttgagacagagttttgctcttgttgccca |
| Fasta
Sequence |
AAGAATGCAC CACTACACTC CAGCCTGCGC GACAGAGTGA AACTGTCTCA AAATAAATAA
ATACATAAAA TTATATGTAT ATATATATAT ATATATATTT TTTTGTATGT GAGACTGGAT
CTCTGTTTCC CAGGCTGGAG TGCAGTGGTG TGATCTCGGC TCACTGCAAC CTCCGCCTCC
TGGGTTCAAG CAATTCTGCC TCAGCCTCCC AAGTAGCTGG GATTATAGGC GTGCGCCACC
ACGCCTGGCT GATTTTTGTA TTTTTAGTAG AGATGGAGTT TCACCATATT ACCCAAGCTG
GTCTTGAACT CCTGACCTCA TGATCCGCCT GCCTCAGCCT CCCAAAGTGC TGAGATTATA
GGGGTGAGCC ACTGTGCCCG GCAATAATAA TTTTTTTTTT
N
TTTGAGACAG AGTTTTGCTC TTGTTGCCCA GGCTGGAGTG CAATGGTGCA ATCTCGGCTC
ACGGCAACCT CCGCCTCTCA TGTTCAAGCT ATTATCCTGA CTCAGCTGGG ATTACAGGCA
CCCACCACCA CACCTGGCTG ATTTTGGTAT TTTTAGTAGA GACGGGGTTT CTCCATGTCG
GCCAGGCTGG TCTCGAACTC CTGACCTCAG GTGATCCACC CGCCTTGGGC TCCCAAAGTG
CTGGGATTAC AGCCCTGAGC CACCATGGCT GACAATAATA AAAAATTTTA AAGCAAAACT
AAAGATTTAT AAATTGTAAA ATGCGGTTGT AACAAGTATT TACTGTACCA GTAAATATGA
AAAATATTAA TGTCCTCACA CACATGGAGG TGGCTTGTGA
|
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