Variant position: 1592 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: 2997 The length of the canonical sequence.
Location on the sequence:
The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human ELMEFSDLESDSEEKPCAKP RRPQDKSQGYARSECFRVEKN
Mouse ELMEFSDLESDSEEKPCAKP RRPQDKSQGYARSECFRVEKN
Chicken ELMEFSDLESDSEEKPSTKP RRPQDKSQGYARSECFRVEKN
Sequence annotation in neighborhood: The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
Type: the type of sequence feature. Positions: endpoints of the sequence feature. Description: contains additional information about the feature.
Type Positions Description
1 – 2997 Chromodomain-helicase-DNA-binding protein 7
1576 – 1600 Disordered
1576 – 1599 Basic and acidic residues
1577 – 1577 Phosphoserine
1581 – 1581 Phosphoserine
572 – 2620 Missing. In isoform 4.
834 – 2620 Missing. In isoform 3.
1139 – 2997 Missing. In isoform 2.
CHD7 mutation spectrum in 28 Swedish patients diagnosed with CHARGE syndrome.
Wincent J.; Holmberg E.; Stromland K.; Soller M.; Mirzaei L.; Djureinovic T.; Robinson K.; Anderlid B.; Schoumans J.;
Clin. Genet. 74:31-38(2008)
Cited for: VARIANTS THR-103 AND ASP-117; VARIANTS CHARGES ARG-1214; PRO-1302; TRP-1592 AND ASP-1742;
Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.