Product Details
- SNP ID
-
rs28934611
- Assay Type
- Functionally tested
- NCBI dbSNP Submissions
-
NA
- Location
-
Chr.X:10449495 on Build GRCh38
- Set Membership
-
- Context Sequence [VIC/FAM]
- CGCAAATGCGACGTCGAAGGTGTAG[A/G]GGTGGATGGAGTTCAAAGCATCATA
- Phenotype
-
MIM: 300552
- Polymorphism
- A/G, Transition substitution
- Allele Nomenclature
-
- Literature Links
-
MID1
PubMed Links
Gene Details
- Gene
- MID1
- Gene Name
- midline 1
Transcript Accession |
SNP Location |
SNP Type |
Codon Change |
Amino Acid Change |
Protein ID |
NM_000381.3 |
2489 |
Missense Mutation |
CCC,CTC |
P626L |
NP_000372.1 |
NM_001098624.2 |
2489 |
Missense Mutation |
CCC,CTC |
P626L |
NP_001092094.1 |
NM_001193277.1 |
2489 |
Missense Mutation |
CCC,CTC |
P626L |
NP_001180206.1 |
NM_001193278.1 |
2489 |
Intron |
|
|
NP_001180207.1 |
NM_001193279.1 |
2489 |
Intron |
|
|
NP_001180208.1 |
NM_001193280.1 |
2489 |
Intron |
|
|
NP_001180209.1 |
NM_001193281.1 |
2489 |
Intron |
|
|
NP_001180210.1 |
NM_033289.1 |
2489 |
Missense Mutation |
CCC,CTC |
P588L |
NP_150631.1 |
NM_033290.3 |
2489 |
Missense Mutation |
CCC,CTC |
P626L |
NP_150632.1 |
XM_005274536.1 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_005274593.1 |
XM_005274537.1 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_005274594.1 |
XM_006724492.3 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_006724555.1 |
XM_011545525.2 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_011543827.1 |
XM_011545526.2 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_011543828.1 |
XM_011545527.2 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_011543829.1 |
XM_017029534.1 |
2489 |
Missense Mutation |
CCC,CTC |
P677L |
XP_016885023.1 |
XM_017029535.1 |
2489 |
Missense Mutation |
CCC,CTC |
P639L |
XP_016885024.1 |
XM_017029536.1 |
2489 |
Missense Mutation |
CCC,CTC |
P626L |
XP_016885025.1 |
XM_017029537.1 |
2489 |
Missense Mutation |
CCC,CTC |
P588L |
XP_016885026.1 |
XM_017029538.1 |
2489 |
Missense Mutation |
CCC,CTC |
P588L |
XP_016885027.1 |
XM_017029539.1 |
2489 |
Missense Mutation |
CCC,CTC |
P588L |
XP_016885028.1 |
XM_017029540.1 |
2489 |
Intron |
|
|
XP_016885029.1 |
XM_017029541.1 |
2489 |
Intron |
|
|
XP_016885030.1 |
XM_017029542.1 |
2489 |
Intron |
|
|
XP_016885031.1 |
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