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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P12111: Variant p.Val1985Met

Collagen alpha-3(VI) chain
Gene: COL6A3
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Variant information Variant position: help 1985 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Valine (V) to Methionine (M) at position 1985 (V1985M, p.Val1985Met). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Similar physico-chemical property. Both residues are medium size and hydrophobic. The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help 1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Variant description: help In BTHLM1C. Any additional useful information about the variant.
Other resources: help Links to websites of interest for the variant.


Sequence information Variant position: help 1985 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 3177 The length of the canonical sequence.
Location on the sequence: help ASENLRQEGVRALILVGLER V VNLERLMHLEFGRGFMYDRP 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: help The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human                         ASENLRQEGVRALILVGLERVVNLERLMHLEFGRGFMYDRP

Chicken                       ASADLRRQGVHALLFVGLDRVKNFEEVMQLEFGRGFTYNRP

Sequence annotation in neighborhood: help 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.
TypePositionsDescription
Chain 26 – 3177 Collagen alpha-3(VI) chain
Domain 1838 – 2024 VWFA 10
Region 26 – 2038 Nonhelical region
Alternative sequence 1444 – 3177 Missing. In isoform 3 and isoform 5.



Literature citations
Automated genomic sequence analysis of the three collagen VI genes: applications to Ullrich congenital muscular dystrophy and Bethlem myopathy.
Lampe A.K.; Dunn D.M.; von Niederhausern A.C.; Hamil C.; Aoyagi A.; Laval S.H.; Marie S.K.; Chu M.-L.; Swoboda K.; Muntoni F.; Bonnemann C.G.; Flanigan K.M.; Bushby K.M.D.; Weiss R.B.;
J. Med. Genet. 42:108-120(2005)
Cited for: VARIANTS BTHLM1C GLU-1014; LYS-1386; ASP-1467; GLU-1679; MET-1985; ASP-2047 AND ASP-2080; VARIANT UCMD1C ASN-1674; VARIANTS VAL-411; HIS-491; SER-492; HIS-677; THR-807; SER-830; GLN-1064; GLN-1088; GLN-1395; GLN-1576; GLN-1632; SER-1687; LEU-2218; HIS-2831 AND VAL-2941;
Disclaimer: 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.