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Table 4 Sequence variants detected in Human ATR and residues found in orthologues

From: Mutation analysis and characterization of ATR sequence variants in breast cancer cases from high-risk French Canadian breast/ovarian cancer families

SNP

SNP ID*

Amino acid change

Pan troglodytes

Canis familiaris

Mus musculus

Xenapus laevis

Fugu rubribes

Strongylocentrotus purpuratus

Drosophila melanogaste

5**

c.632C>T

Thr211 Met

Thr

Thr

Met

Met

Gly

-

Glu

6

c. 946G>A

Va1316Ile

Val

Val

Val

Val

Val

Ser

Asp

14

c. 2290A>G

Lys764Glu

Lys

Lys

Lys

Lys

Lys

Ser

Glu

16

c. 2875G>A

Val959Met

Met

Met

Ile

Met

Ser

Thr

Phe

34

c. 6394T>G

Tyr2132Asp

Tyr

His

Arg

Gln

Asn

Lys

Ala

39

c. 7274G>A

Arg2425Gln

-

Arg

Gln

Lys

Lys

Glu

Thr

  1. * According to the nomenclature of the Human Genome Variation Society
  2. - No corresponding residue in this species
  3. ** T allele is considered as the common allele according to the reference sequence NM_001184