Product Details

SNP ID
rs6640649
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.X:10450220 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TAAGTTAAATGATTTAAATAGCTGC[A/C]TGTGGCTCATAGCTACCATACTGGA
Phenotype
MIM: 300552
Polymorphism
A/C, Transversion 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 Intron NP_000372.1
NM_001098624.2 Intron NP_001092094.1
NM_001193277.1 Intron NP_001180206.1
NM_001193278.1 Intron NP_001180207.1
NM_001193279.1 Intron NP_001180208.1
NM_001193280.1 Intron NP_001180209.1
NM_001193281.1 Intron NP_001180210.1
NM_033289.1 Intron NP_150631.1
NM_033290.3 Intron NP_150632.1
XM_005274536.1 Intron XP_005274593.1
XM_005274537.1 Intron XP_005274594.1
XM_006724492.3 Intron XP_006724555.1
XM_011545525.2 Intron XP_011543827.1
XM_011545526.2 Intron XP_011543828.1
XM_011545527.2 Intron XP_011543829.1
XM_017029534.1 Intron XP_016885023.1
XM_017029535.1 Intron XP_016885024.1
XM_017029536.1 Intron XP_016885025.1
XM_017029537.1 Intron XP_016885026.1
XM_017029538.1 Intron XP_016885027.1
XM_017029539.1 Intron XP_016885028.1
XM_017029540.1 Intron XP_016885029.1
XM_017029541.1 Intron XP_016885030.1
XM_017029542.1 Intron XP_016885031.1

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