Product Details

SNP ID

rs150291968

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:10449484 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAAACAGGCTGCGCAAATGCGACGT[C/T]GAAGGTGTAGAGGTGGATGGAGTTC

Phenotype

MIM: 300552

Polymorphism

C/T, 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	2500	Missense Mutation	AAC,GAC	N630D	NP_000372.1
NM_001098624.2	2500	Missense Mutation	AAC,GAC	N630D	NP_001092094.1
NM_001193277.1	2500	Missense Mutation	AAC,GAC	N630D	NP_001180206.1
NM_001193278.1	2500	Intron			NP_001180207.1
NM_001193279.1	2500	Intron			NP_001180208.1
NM_001193280.1	2500	Intron			NP_001180209.1
NM_001193281.1	2500	Intron			NP_001180210.1
NM_033289.1	2500	Missense Mutation	AAC,GAC	N592D	NP_150631.1
NM_033290.3	2500	Missense Mutation	AAC,GAC	N630D	NP_150632.1
XM_005274536.1	2500	Missense Mutation	AAC,GAC	N681D	XP_005274593.1
XM_005274537.1	2500	Missense Mutation	AAC,GAC	N681D	XP_005274594.1
XM_006724492.3	2500	Missense Mutation	AAC,GAC	N681D	XP_006724555.1
XM_011545525.2	2500	Missense Mutation	AAC,GAC	N681D	XP_011543827.1
XM_011545526.2	2500	Missense Mutation	AAC,GAC	N681D	XP_011543828.1
XM_011545527.2	2500	Missense Mutation	AAC,GAC	N681D	XP_011543829.1
XM_017029534.1	2500	Missense Mutation	AAC,GAC	N681D	XP_016885023.1
XM_017029535.1	2500	Missense Mutation	AAC,GAC	N643D	XP_016885024.1
XM_017029536.1	2500	Missense Mutation	AAC,GAC	N630D	XP_016885025.1
XM_017029537.1	2500	Missense Mutation	AAC,GAC	N592D	XP_016885026.1
XM_017029538.1	2500	Missense Mutation	AAC,GAC	N592D	XP_016885027.1
XM_017029539.1	2500	Missense Mutation	AAC,GAC	N592D	XP_016885028.1
XM_017029540.1	2500	Intron			XP_016885029.1
XM_017029541.1	2500	Intron			XP_016885030.1
XM_017029542.1	2500	Intron			XP_016885031.1

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